|
NM_002019.4:c.3174+225T>G
MANE Select
|
NP_002010.2:n.3174+225T>G
|
|
ENST00000282397.9:c.3174+225T>G
MANE Select
|
ENSP00000282397.4:n.3174+225T>G
|
|
ENST00000282397.8:c.3174+225T>G
|
ENSP00000282397.4:n.3174+225T>G
|
|
ENST00000540678.2:c.-586+225T>G
|
ENSP00000443311.2:n.-586+225T>G
|
|
ENST00000543394.2:c.243+225T>G
|
ENSP00000437841.1:n.243+225T>G
|
|
ENST00000615611.4:c.459+225T>G
|
ENSP00000484385.1:n.459+225T>G
|
|
ENST00000706527.1:n.999+225T>G
|
|
|
XM_017020485.1:c.3060+225T>G
|
XP_016875974.1:n.3060+225T>G
|
|
XR_941798.1:n.918-7383A>C
|
|