ENST00000519602.6:c.667+2T>C
MANE Select
|
ENSP00000430055.2:n.667+2T>C
|
|
ENST00000323997.10:c.667+2T>C
|
ENSP00000324105.6:n.667+2T>C
|
|
ENST00000518175.1:c.667+2T>C
|
ENSP00000431087.1:n.667+2T>C
|
|
ENST00000519584.5:c.538+2T>C
|
ENSP00000430636.1:n.538+2T>C
|
|
ENST00000519602.5:c.667+2T>C
|
ENSP00000430055.1:n.667+2T>C
|
|
ENST00000521659.5:c.*613+2T>C
|
ENSP00000430554.1:n.*613+2T>C
|
|
NM_001193503.1:c.538+2T>C
|
NP_001180432.1:n.538+2T>C
|
|
NM_001976.4:c.667+2T>C
|
NP_001967.3:n.667+2T>C
|
|
NM_053013.3:c.667+2T>C
|
NP_443739.3:n.667+2T>C
|
|
XM_005256521.2:c.694+2T>C
|
XP_005256578.1:n.694+2T>C
|
|
XM_011523729.1:c.667+2T>C
|
XP_011522031.1:n.667+2T>C
|
|
XM_017024346.2:c.667+2T>C
|
XP_016879835.1:n.667+2T>C
|
|
NM_001193503.2:c.538+2T>C
|
NP_001180432.1:n.538+2T>C
|
|
NM_001374523.1:c.667+2T>C
|
NP_001361452.1:n.667+2T>C
|
|
NM_001374524.1:c.694+2T>C
|
NP_001361453.1:n.694+2T>C
|
|
NM_001976.5:c.667+2T>C
|
NP_001967.3:n.667+2T>C
|
|
NM_053013.4:c.667+2T>C
MANE Select
|
NP_443739.3:n.667+2T>C
|
|