ENST00000322953.9:c.70+3781G>C
MANE Select
|
ENSP00000320509.4:n.70+3781G>C
|
|
ENST00000322953.8:c.70+3781G>C
|
ENSP00000320509.4:n.70+3781G>C
|
|
ENST00000428908.5:c.70+3781G>C
|
ENSP00000412748.1:n.70+3781G>C
|
|
ENST00000504592.5:c.26-35077G>C
|
ENSP00000421443.1:n.26-35077G>C
|
|
ENST00000508653.5:c.70+3781G>C
|
ENSP00000422314.1:n.70+3781G>C
|
|
NM_001127507.2:c.70+3781G>C
|
NP_001120979.2:n.70+3781G>C
|
|
NM_017935.4:c.70+3781G>C
|
NP_060405.4:n.70+3781G>C
|
|
XM_017008337.2:c.-21+4159G>C
|
XP_016863826.1:n.-21+4159G>C
|
|
NM_017935.5:c.70+3781G>C
MANE Select
|
NP_060405.5:n.70+3781G>C
|
|
NM_001127507.3:c.70+3781G>C
|
NP_001120979.3:n.70+3781G>C
|
|