ENST00000264380.9:c.3590T>G
MANE Select
|
ENSP00000264380.4:p.Ile1197Ser
|
|
ENST00000264380.8:c.3590T>G
|
ENSP00000264380.4:p.Ile1197Ser
|
|
ENST00000452564.1:c.3422T>G
|
ENSP00000405736.1:p.Ile1141Ser
|
|
NM_015040.3:c.3590T>G
|
NP_055855.2:p.Ile1197Ser
|
|
XM_011510778.1:c.3626T>G
|
XP_011509080.1:p.Ile1209Ser
|
|
XM_011510779.1:c.3626T>G
|
XP_011509081.1:p.Ile1209Ser
|
|
XM_011510780.1:c.3623T>G
|
XP_011509082.1:p.Ile1208Ser
|
|
XM_011510781.1:c.3608T>G
|
XP_011509083.1:p.Ile1203Ser
|
|
XM_011510782.1:c.3626T>G
|
XP_011509084.1:p.Ile1209Ser
|
|
XM_011510783.1:c.3458T>G
|
XP_011509085.1:p.Ile1153Ser
|
|
XM_011510784.1:c.3455T>G
|
XP_011509086.1:p.Ile1152Ser
|
|
XM_011510785.1:c.3440T>G
|
XP_011509087.1:p.Ile1147Ser
|
|
XM_011510786.1:c.3335T>G
|
XP_011509088.1:p.Ile1112Ser
|
|
XM_011510787.1:c.3332T>G
|
XP_011509089.1:p.Ile1111Ser
|
|
XM_011510788.1:c.3299T>G
|
XP_011509090.1:p.Ile1100Ser
|
|
XM_011510789.1:c.3149T>G
|
XP_011509091.1:p.Ile1050Ser
|
|
XM_011510790.1:c.2633T>G
|
XP_011509092.1:p.Ile878Ser
|
|
XM_011510791.1:c.2633T>G
|
XP_011509093.1:p.Ile878Ser
|
|
XM_011510792.1:c.3626T>G
|
XP_011509094.1:p.Ile1209Ser
|
|
XR_922888.1:n.3763T>G
|
|
|
XM_011510778.3:c.3626T>G
|
XP_011509080.1:p.Ile1209Ser
|
|
XM_011510779.2:c.3626T>G
|
XP_011509081.1:p.Ile1209Ser
|
|
XM_011510780.2:c.3623T>G
|
XP_011509082.1:p.Ile1208Ser
|
|
XM_011510781.3:c.3608T>G
|
XP_011509083.1:p.Ile1203Ser
|
|
XM_011510782.3:c.3626T>G
|
XP_011509084.1:p.Ile1209Ser
|
|
XM_011510783.3:c.3458T>G
|
XP_011509085.1:p.Ile1153Ser
|
|
XM_011510784.2:c.3455T>G
|
XP_011509086.1:p.Ile1152Ser
|
|
XM_011510785.3:c.3440T>G
|
XP_011509087.1:p.Ile1147Ser
|
|
XM_011510786.3:c.3335T>G
|
XP_011509088.1:p.Ile1112Ser
|
|
XM_011510789.2:c.3149T>G
|
XP_011509091.1:p.Ile1050Ser
|
|
XM_011510792.3:c.3626T>G
|
XP_011509094.1:p.Ile1209Ser
|
|
XM_017003568.1:c.3572T>G
|
XP_016859057.1:p.Ile1191Ser
|
|
XM_017003569.1:c.3404T>G
|
XP_016859058.1:p.Ile1135Ser
|
|
XM_017003570.1:c.3131T>G
|
XP_016859059.1:p.Ile1044Ser
|
|
XM_017003571.1:c.2981T>G
|
XP_016859060.1:p.Ile994Ser
|
|
XM_017003572.1:c.2633T>G
|
XP_016859061.1:p.Ile878Ser
|
|
XM_017003573.1:c.2633T>G
|
XP_016859062.1:p.Ile878Ser
|
|
XM_017003574.1:c.2633T>G
|
XP_016859063.1:p.Ile878Ser
|
|
NM_015040.4:c.3590T>G
MANE Select
|
NP_055855.2:p.Ile1197Ser
|
|