ENST00000013070.11:c.602-129G>C
MANE Select
|
ENSP00000013070.6:n.602-129G>C
|
|
ENST00000013070.10:c.602-129G>C
|
ENSP00000013070.6:n.602-129G>C
|
|
ENST00000416753.5:c.374-129G>C
|
ENSP00000391706.2:n.374-129G>C
|
|
ENST00000553674.1:c.*303-129G>C
|
ENSP00000450470.1:n.*303-129G>C
|
|
ENST00000553857.5:c.378+3117G>C
|
|
|
ENST00000554232.5:c.506-129G>C
|
ENSP00000450645.1:n.506-129G>C
|
|
ENST00000556871.5:c.311-129G>C
|
ENSP00000451022.1:n.311-129G>C
|
|
ENST00000557048.1:n.511-129G>C
|
|
|
NM_175748.3:c.602-129G>C
|
NP_786924.2:n.602-129G>C
|
|
NR_038150.1:n.704-129G>C
|
|
|
NM_175748.4:c.602-129G>C
MANE Select
|
NP_786924.2:n.602-129G>C
|
|
NR_038150.2:n.504-129G>C
|
|
|