ENST00000697291.1:c.*903G>T
|
ENSP00000513228.1:n.*903G>T
|
|
ENST00000648433.1:c.1306G>T
|
ENSP00000496816.1:p.Asp436Tyr
|
|
ENST00000649554.1:n.916G>T
|
|
|
ENST00000649979.2:c.1306G>T
MANE Select
|
ENSP00000497271.1:p.Asp436Tyr
|
|
ENST00000679938.1:c.994G>T
|
ENSP00000505518.1:p.Asp332Tyr
|
|
ENST00000263642.2:c.1306G>T
|
ENSP00000263642.2:p.Asp436Tyr
|
|
NM_022168.3:c.1306G>T
|
NP_071451.2:p.Asp436Tyr
|
|
XM_011511628.1:c.589G>T
|
XP_011509930.1:p.Asp197Tyr
|
|
XM_011511629.1:c.1306G>T
|
XP_011509931.1:p.Asp436Tyr
|
|
NM_022168.4:c.1306G>T
MANE Select
|
NP_071451.2:p.Asp436Tyr
|
|