ENST00000264380.9:c.3465T>G
MANE Select
|
ENSP00000264380.4:p.Tyr1155Ter
|
|
ENST00000264380.8:c.3465T>G
|
ENSP00000264380.4:p.Tyr1155Ter
|
|
ENST00000452564.1:c.3297T>G
|
ENSP00000405736.1:p.Tyr1099Ter
|
|
NM_015040.3:c.3465T>G
|
NP_055855.2:p.Tyr1155Ter
|
|
XM_011510778.1:c.3501T>G
|
XP_011509080.1:p.Tyr1167Ter
|
|
XM_011510779.1:c.3501T>G
|
XP_011509081.1:p.Tyr1167Ter
|
|
XM_011510780.1:c.3498T>G
|
XP_011509082.1:p.Tyr1166Ter
|
|
XM_011510781.1:c.3483T>G
|
XP_011509083.1:p.Tyr1161Ter
|
|
XM_011510782.1:c.3501T>G
|
XP_011509084.1:p.Tyr1167Ter
|
|
XM_011510783.1:c.3333T>G
|
XP_011509085.1:p.Tyr1111Ter
|
|
XM_011510784.1:c.3330T>G
|
XP_011509086.1:p.Tyr1110Ter
|
|
XM_011510785.1:c.3315T>G
|
XP_011509087.1:p.Tyr1105Ter
|
|
XM_011510786.1:c.3210T>G
|
XP_011509088.1:p.Tyr1070Ter
|
|
XM_011510787.1:c.3207T>G
|
XP_011509089.1:p.Tyr1069Ter
|
|
XM_011510788.1:c.3174T>G
|
XP_011509090.1:p.Tyr1058Ter
|
|
XM_011510789.1:c.3024T>G
|
XP_011509091.1:p.Tyr1008Ter
|
|
XM_011510790.1:c.2508T>G
|
XP_011509092.1:p.Tyr836Ter
|
|
XM_011510791.1:c.2508T>G
|
XP_011509093.1:p.Tyr836Ter
|
|
XM_011510792.1:c.3501T>G
|
XP_011509094.1:p.Tyr1167Ter
|
|
XR_922888.1:n.3638T>G
|
|
|
XM_011510778.3:c.3501T>G
|
XP_011509080.1:p.Tyr1167Ter
|
|
XM_011510779.2:c.3501T>G
|
XP_011509081.1:p.Tyr1167Ter
|
|
XM_011510780.2:c.3498T>G
|
XP_011509082.1:p.Tyr1166Ter
|
|
XM_011510781.3:c.3483T>G
|
XP_011509083.1:p.Tyr1161Ter
|
|
XM_011510782.3:c.3501T>G
|
XP_011509084.1:p.Tyr1167Ter
|
|
XM_011510783.3:c.3333T>G
|
XP_011509085.1:p.Tyr1111Ter
|
|
XM_011510784.2:c.3330T>G
|
XP_011509086.1:p.Tyr1110Ter
|
|
XM_011510785.3:c.3315T>G
|
XP_011509087.1:p.Tyr1105Ter
|
|
XM_011510786.3:c.3210T>G
|
XP_011509088.1:p.Tyr1070Ter
|
|
XM_011510789.2:c.3024T>G
|
XP_011509091.1:p.Tyr1008Ter
|
|
XM_011510792.3:c.3501T>G
|
XP_011509094.1:p.Tyr1167Ter
|
|
XM_017003568.1:c.3447T>G
|
XP_016859057.1:p.Tyr1149Ter
|
|
XM_017003569.1:c.3279T>G
|
XP_016859058.1:p.Tyr1093Ter
|
|
XM_017003570.1:c.3006T>G
|
XP_016859059.1:p.Tyr1002Ter
|
|
XM_017003571.1:c.2856T>G
|
XP_016859060.1:p.Tyr952Ter
|
|
XM_017003572.1:c.2508T>G
|
XP_016859061.1:p.Tyr836Ter
|
|
XM_017003573.1:c.2508T>G
|
XP_016859062.1:p.Tyr836Ter
|
|
XM_017003574.1:c.2508T>G
|
XP_016859063.1:p.Tyr836Ter
|
|
NM_015040.4:c.3465T>G
MANE Select
|
NP_055855.2:p.Tyr1155Ter
|
|