ENST00000695651.1:n.2670G>C
|
|
|
ENST00000695653.1:c.2231G>C
|
ENSP00000512084.1:p.Arg744Thr
|
|
ENST00000695654.1:c.3347G>C
|
ENSP00000512085.1:p.Arg1116Thr
|
|
ENST00000695689.1:c.293G>C
|
ENSP00000512101.1:n.293G>C
|
|
ENST00000695690.1:n.513G>C
|
|
|
ENST00000695691.1:n.513G>C
|
|
|
ENST00000245907.11:c.4322G>C
MANE Select
|
ENSP00000245907.4:p.Arg1441Thr
|
|
ENST00000245907.10:c.4322G>C
|
ENSP00000245907.4:p.Arg1441Thr
|
|
ENST00000596548.1:c.443G>C
|
ENSP00000469744.1:p.Arg148Thr
|
|
ENST00000599899.5:n.1281G>C
|
|
|
ENST00000601008.1:c.242-4011G>C
|
ENSP00000471384.1:n.242-4011G>C
|
|
NM_000064.3:c.4322G>C
|
NP_000055.2:p.Arg1441Thr
|
|
NM_000064.4:c.4322G>C
MANE Select
|
NP_000055.2:p.Arg1441Thr
|
|