ENST00000703783.1:n.308T>A
|
|
|
ENST00000703785.1:n.389T>A
|
|
|
ENST00000262464.9:c.3524T>A
MANE Select
|
ENSP00000262464.4:p.Val1175Glu
|
|
ENST00000262464.8:c.3524T>A
|
ENSP00000262464.4:p.Val1175Glu
|
|
ENST00000507835.5:c.74T>A
|
ENSP00000426839.1:p.Val25Glu
|
|
ENST00000508053.5:c.3524T>A
|
ENSP00000424571.1:p.Val1175Glu
|
|
ENST00000508989.5:c.3425T>A
|
ENSP00000425596.1:p.Val1142Glu
|
|
ENST00000619499.4:c.3521T>A
|
ENSP00000482132.1:p.Val1174Glu
|
|
NM_001999.3:c.3524T>A
|
NP_001990.2:p.Val1175Glu
|
|
XM_017009228.2:c.3371T>A
|
XP_016864717.1:p.Val1124Glu
|
|
NM_001999.4:c.3524T>A
MANE Select
|
NP_001990.2:p.Val1175Glu
|
|