ENST00000366667.6:c.1242+7G>T
MANE Select
|
ENSP00000355627.5:n.1242+7G>T
|
|
ENST00000679684.1:c.1242+7G>T
|
ENSP00000505981.1:n.1242+7G>T
|
|
ENST00000679738.1:c.1242+7G>T
|
ENSP00000505063.1:n.1242+7G>T
|
|
ENST00000679802.1:c.*701+7G>T
|
ENSP00000505184.1:n.*701+7G>T
|
|
ENST00000679854.1:n.5547+7G>T
|
|
|
ENST00000679957.1:c.1233+16G>T
|
ENSP00000506646.1:n.1233+16G>T
|
|
ENST00000680041.1:c.1242+7G>T
|
ENSP00000504866.1:n.1242+7G>T
|
|
ENST00000680783.1:c.829+5809G>T
|
ENSP00000506329.1:n.829+5809G>T
|
|
ENST00000681269.1:c.1242+7G>T
|
ENSP00000505985.1:n.1242+7G>T
|
|
ENST00000681347.1:n.3348+7G>T
|
|
|
ENST00000681514.1:c.1242+7G>T
|
ENSP00000505963.1:n.1242+7G>T
|
|
ENST00000681772.1:c.*736+7G>T
|
ENSP00000505829.1:n.*736+7G>T
|
|
ENST00000366667.4:c.1269+7G>T
|
ENSP00000355627.4:n.1269+7G>T
|
|
NM_000029.3:c.1269+7G>T
|
NP_000020.1:n.1269+7G>T
|
|
NM_000029.4:c.1269+7G>T
|
NP_000020.1:n.1269+7G>T
|
|
NM_001382817.3:c.1242+7G>T
|
NP_001369746.2:n.1242+7G>T
|
|
NM_001384479.1:c.1242+7G>T
MANE Select
|
NP_001371408.1:n.1242+7G>T
|
|