ENST00000695651.1:n.2528G>C
|
|
|
ENST00000695653.1:c.2089G>C
|
ENSP00000512084.1:p.Gly697Arg
|
|
ENST00000695654.1:c.3205G>C
|
ENSP00000512085.1:p.Gly1069Arg
|
|
ENST00000695689.1:c.151G>C
|
ENSP00000512101.1:n.151G>C
|
|
ENST00000695690.1:n.371G>C
|
|
|
ENST00000695691.1:n.371G>C
|
|
|
ENST00000245907.11:c.4180G>C
MANE Select
|
ENSP00000245907.4:p.Gly1394Arg
|
|
ENST00000245907.10:c.4180G>C
|
ENSP00000245907.4:p.Gly1394Arg
|
|
ENST00000596548.1:c.301G>C
|
ENSP00000469744.1:p.Gly101Arg
|
|
ENST00000599899.5:n.1139G>C
|
|
|
ENST00000601008.1:c.242-4264G>C
|
ENSP00000471384.1:n.242-4264G>C
|
|
NM_000064.3:c.4180G>C
|
NP_000055.2:p.Gly1394Arg
|
|
NM_000064.4:c.4180G>C
MANE Select
|
NP_000055.2:p.Gly1394Arg
|
|