ENST00000547103.7:c.6114T>C
MANE Select
|
ENSP00000447211.2:p.Tyr2038=
|
|
ENST00000642294.1:c.54T>C
|
ENSP00000493572.1:p.Tyr18=
|
|
ENST00000646859.1:c.5979T>C
|
ENSP00000496036.1:p.Tyr1993=
|
|
ENST00000298820.7:c.1415T>C
|
|
|
ENST00000458043.6:c.6087T>C
|
ENSP00000400895.2:p.Tyr2029=
|
|
ENST00000546620.5:n.370T>C
|
|
|
ENST00000547103.5:c.6051T>C
|
ENSP00000447211.1:p.Tyr2017=
|
|
ENST00000550182.2:c.138T>C
|
ENSP00000449641.1:p.Tyr46=
|
|
ENST00000551340.5:c.242T>C
|
|
|
NM_173591.3:c.6087T>C
|
NP_775862.3:p.Tyr2029=
|
|
XM_005268802.2:c.6138T>C
|
XP_005268859.1:p.Tyr2046=
|
|
XM_011538191.1:c.6138T>C
|
XP_011536493.1:p.Tyr2046=
|
|
XM_011538192.1:c.5985T>C
|
XP_011536494.1:p.Tyr1995=
|
|
XM_011538193.1:c.5772T>C
|
XP_011536495.1:p.Tyr1924=
|
|
XM_005268802.3:c.6138T>C
|
XP_005268859.1:p.Tyr2046=
|
|
XM_011538192.2:c.5985T>C
|
XP_011536494.1:p.Tyr1995=
|
|
NM_001368062.1:c.5952T>C
|
NP_001354991.1:p.Tyr1984=
|
|
NM_001368062.3:c.5979T>C
|
NP_001354991.2:p.Tyr1993=
|
|
NM_001378609.3:c.6114T>C
MANE Select
|
NP_001365538.2:p.Tyr2038=
|
|
NM_001378610.3:c.6114T>C
|
NP_001365539.2:p.Tyr2038=
|
|
NM_173591.7:c.6114T>C
|
NP_775862.4:p.Tyr2038=
|
|