ENST00000703783.1:n.316G>T
|
|
|
ENST00000703785.1:n.397G>T
|
|
|
ENST00000262464.9:c.3532G>T
MANE Select
|
ENSP00000262464.4:p.Glu1178Ter
|
|
ENST00000262464.8:c.3532G>T
|
ENSP00000262464.4:p.Glu1178Ter
|
|
ENST00000507835.5:c.82G>T
|
ENSP00000426839.1:p.Glu28Ter
|
|
ENST00000508053.5:c.3532G>T
|
ENSP00000424571.1:p.Glu1178Ter
|
|
ENST00000508989.5:c.3433G>T
|
ENSP00000425596.1:p.Glu1145Ter
|
|
ENST00000619499.4:c.3529G>T
|
ENSP00000482132.1:p.Glu1177Ter
|
|
NM_001999.3:c.3532G>T
|
NP_001990.2:p.Glu1178Ter
|
|
XM_017009228.2:c.3379G>T
|
XP_016864717.1:p.Glu1127Ter
|
|
NM_001999.4:c.3532G>T
MANE Select
|
NP_001990.2:p.Glu1178Ter
|
|