ENST00000264380.9:c.3441_3442delinsCT
MANE Select
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ENSP00000264380.4:p.Ser1147=
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ENST00000264380.8:c.3441_3442delinsCT
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ENSP00000264380.4:p.Ser1147=
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ENST00000452564.1:c.3273_3274delinsCT
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ENSP00000405736.1:p.Ser1091=
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NM_015040.3:c.3441_3442delinsCT
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NP_055855.2:p.Ser1147=
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XM_011510778.1:c.3477_3478delinsCT
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XP_011509080.1:p.Ser1159=
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XM_011510779.1:c.3477_3478delinsCT
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XP_011509081.1:p.Ser1159=
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XM_011510780.1:c.3474_3475delinsCT
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XP_011509082.1:p.Ser1158=
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XM_011510781.1:c.3459_3460delinsCT
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XP_011509083.1:p.Ser1153=
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XM_011510782.1:c.3477_3478delinsCT
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XP_011509084.1:p.Ser1159=
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XM_011510783.1:c.3309_3310delinsCT
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XP_011509085.1:p.Ser1103=
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XM_011510784.1:c.3306_3307delinsCT
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XP_011509086.1:p.Ser1102=
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XM_011510785.1:c.3291_3292delinsCT
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XP_011509087.1:p.Ser1097=
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XM_011510786.1:c.3186_3187delinsCT
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XP_011509088.1:p.Ser1062=
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XM_011510787.1:c.3183_3184delinsCT
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XP_011509089.1:p.Ser1061=
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XM_011510788.1:c.3150_3151delinsCT
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XP_011509090.1:p.Ser1050=
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XM_011510789.1:c.3000_3001delinsCT
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XP_011509091.1:p.Ser1000=
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XM_011510790.1:c.2484_2485delinsCT
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XP_011509092.1:p.Ser828=
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XM_011510791.1:c.2484_2485delinsCT
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XP_011509093.1:p.Ser828=
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XM_011510792.1:c.3477_3478delinsCT
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XP_011509094.1:p.Ser1159=
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XR_922888.1:n.3614_3615delinsCT
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XM_011510778.3:c.3477_3478delinsCT
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XP_011509080.1:p.Ser1159=
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XM_011510779.2:c.3477_3478delinsCT
|
XP_011509081.1:p.Ser1159=
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|
XM_011510780.2:c.3474_3475delinsCT
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XP_011509082.1:p.Ser1158=
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|
XM_011510781.3:c.3459_3460delinsCT
|
XP_011509083.1:p.Ser1153=
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XM_011510782.3:c.3477_3478delinsCT
|
XP_011509084.1:p.Ser1159=
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|
XM_011510783.3:c.3309_3310delinsCT
|
XP_011509085.1:p.Ser1103=
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|
XM_011510784.2:c.3306_3307delinsCT
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XP_011509086.1:p.Ser1102=
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XM_011510785.3:c.3291_3292delinsCT
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XP_011509087.1:p.Ser1097=
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XM_011510786.3:c.3186_3187delinsCT
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XP_011509088.1:p.Ser1062=
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XM_011510789.2:c.3000_3001delinsCT
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XP_011509091.1:p.Ser1000=
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|
XM_011510792.3:c.3477_3478delinsCT
|
XP_011509094.1:p.Ser1159=
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|
XM_017003568.1:c.3423_3424delinsCT
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XP_016859057.1:p.Ser1141=
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XM_017003569.1:c.3255_3256delinsCT
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XP_016859058.1:p.Ser1085=
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XM_017003570.1:c.2982_2983delinsCT
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XP_016859059.1:p.Ser994=
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|
XM_017003571.1:c.2832_2833delinsCT
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XP_016859060.1:p.Ser944=
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XM_017003572.1:c.2484_2485delinsCT
|
XP_016859061.1:p.Ser828=
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|
XM_017003573.1:c.2484_2485delinsCT
|
XP_016859062.1:p.Ser828=
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XM_017003574.1:c.2484_2485delinsCT
|
XP_016859063.1:p.Ser828=
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NM_015040.4:c.3441_3442delinsCT
MANE Select
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NP_055855.2:p.Ser1147=
|
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