ENST00000264380.9:c.3469G>T
MANE Select
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ENSP00000264380.4:p.Ala1157Ser
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ENST00000264380.8:c.3469G>T
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ENSP00000264380.4:p.Ala1157Ser
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|
ENST00000452564.1:c.3301G>T
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ENSP00000405736.1:p.Ala1101Ser
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NM_015040.3:c.3469G>T
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NP_055855.2:p.Ala1157Ser
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XM_011510778.1:c.3505G>T
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XP_011509080.1:p.Ala1169Ser
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XM_011510779.1:c.3505G>T
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XP_011509081.1:p.Ala1169Ser
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|
XM_011510780.1:c.3502G>T
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XP_011509082.1:p.Ala1168Ser
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XM_011510781.1:c.3487G>T
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XP_011509083.1:p.Ala1163Ser
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|
XM_011510782.1:c.3505G>T
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XP_011509084.1:p.Ala1169Ser
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|
XM_011510783.1:c.3337G>T
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XP_011509085.1:p.Ala1113Ser
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XM_011510784.1:c.3334G>T
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XP_011509086.1:p.Ala1112Ser
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XM_011510785.1:c.3319G>T
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XP_011509087.1:p.Ala1107Ser
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|
XM_011510786.1:c.3214G>T
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XP_011509088.1:p.Ala1072Ser
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XM_011510787.1:c.3211G>T
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XP_011509089.1:p.Ala1071Ser
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XM_011510788.1:c.3178G>T
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XP_011509090.1:p.Ala1060Ser
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|
XM_011510789.1:c.3028G>T
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XP_011509091.1:p.Ala1010Ser
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XM_011510790.1:c.2512G>T
|
XP_011509092.1:p.Ala838Ser
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|
XM_011510791.1:c.2512G>T
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XP_011509093.1:p.Ala838Ser
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|
XM_011510792.1:c.3505G>T
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XP_011509094.1:p.Ala1169Ser
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|
XR_922888.1:n.3642G>T
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|
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XM_011510778.3:c.3505G>T
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XP_011509080.1:p.Ala1169Ser
|
|
XM_011510779.2:c.3505G>T
|
XP_011509081.1:p.Ala1169Ser
|
|
XM_011510780.2:c.3502G>T
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XP_011509082.1:p.Ala1168Ser
|
|
XM_011510781.3:c.3487G>T
|
XP_011509083.1:p.Ala1163Ser
|
|
XM_011510782.3:c.3505G>T
|
XP_011509084.1:p.Ala1169Ser
|
|
XM_011510783.3:c.3337G>T
|
XP_011509085.1:p.Ala1113Ser
|
|
XM_011510784.2:c.3334G>T
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XP_011509086.1:p.Ala1112Ser
|
|
XM_011510785.3:c.3319G>T
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XP_011509087.1:p.Ala1107Ser
|
|
XM_011510786.3:c.3214G>T
|
XP_011509088.1:p.Ala1072Ser
|
|
XM_011510789.2:c.3028G>T
|
XP_011509091.1:p.Ala1010Ser
|
|
XM_011510792.3:c.3505G>T
|
XP_011509094.1:p.Ala1169Ser
|
|
XM_017003568.1:c.3451G>T
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XP_016859057.1:p.Ala1151Ser
|
|
XM_017003569.1:c.3283G>T
|
XP_016859058.1:p.Ala1095Ser
|
|
XM_017003570.1:c.3010G>T
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XP_016859059.1:p.Ala1004Ser
|
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XM_017003571.1:c.2860G>T
|
XP_016859060.1:p.Ala954Ser
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XM_017003572.1:c.2512G>T
|
XP_016859061.1:p.Ala838Ser
|
|
XM_017003573.1:c.2512G>T
|
XP_016859062.1:p.Ala838Ser
|
|
XM_017003574.1:c.2512G>T
|
XP_016859063.1:p.Ala838Ser
|
|
NM_015040.4:c.3469G>T
MANE Select
|
NP_055855.2:p.Ala1157Ser
|
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