ENST00000703783.1:n.198T=
|
|
|
ENST00000703785.1:n.279T=
|
|
|
ENST00000262464.9:c.3414T=
MANE Select
|
ENSP00000262464.4:p.Phe1138=
|
|
ENST00000262464.8:c.3414T=
|
ENSP00000262464.4:p.Phe1138=
|
|
ENST00000507835.5:c.-37T=
|
ENSP00000426839.1:n.-37T=
|
|
ENST00000508053.5:c.3414T=
|
ENSP00000424571.1:p.Phe1138=
|
|
ENST00000508989.5:c.3315T=
|
ENSP00000425596.1:p.Phe1105=
|
|
ENST00000619499.4:c.3411T=
|
ENSP00000482132.1:p.Phe1137=
|
|
NM_001999.3:c.3414T=
|
NP_001990.2:p.Phe1138=
|
|
XM_017009228.2:c.3261T=
|
XP_016864717.1:p.Phe1087=
|
|
NM_001999.4:c.3414T=
MANE Select
|
NP_001990.2:p.Phe1138=
|
|