ENST00000703783.1:n.1096G>T
|
|
|
ENST00000703785.1:n.1177G>T
|
|
|
ENST00000262464.9:c.4312G>T
MANE Select
|
ENSP00000262464.4:p.Glu1438Ter
|
|
ENST00000262464.8:c.4312G>T
|
ENSP00000262464.4:p.Glu1438Ter
|
|
ENST00000507835.5:c.862G>T
|
ENSP00000426839.1:p.Glu288Ter
|
|
ENST00000508053.5:c.4312G>T
|
ENSP00000424571.1:p.Glu1438Ter
|
|
ENST00000508989.5:c.4213G>T
|
ENSP00000425596.1:p.Glu1405Ter
|
|
ENST00000619499.4:c.4309G>T
|
ENSP00000482132.1:p.Glu1437Ter
|
|
NM_001999.3:c.4312G>T
|
NP_001990.2:p.Glu1438Ter
|
|
XM_017009228.2:c.4159G>T
|
XP_016864717.1:p.Glu1387Ter
|
|
NM_001999.4:c.4312G>T
MANE Select
|
NP_001990.2:p.Glu1438Ter
|
|