ENST00000695651.1:n.2158+127T>C
|
|
|
ENST00000695653.1:c.1719+127T>C
|
ENSP00000512084.1:n.1719+127T>C
|
|
ENST00000695654.1:c.2835+127T>C
|
ENSP00000512085.1:n.2835+127T>C
|
|
ENST00000245907.11:c.3810+127T>C
MANE Select
|
ENSP00000245907.4:n.3810+127T>C
|
|
ENST00000245907.10:c.3810+127T>C
|
ENSP00000245907.4:n.3810+127T>C
|
|
ENST00000596238.1:n.253+127T>C
|
|
|
ENST00000601008.1:c.241+749T>C
|
ENSP00000471384.1:n.241+749T>C
|
|
NM_000064.3:c.3810+127T>C
|
NP_000055.2:n.3810+127T>C
|
|
NM_000064.4:c.3810+127T>C
MANE Select
|
NP_000055.2:n.3810+127T>C
|
|