ENST00000695651.1:n.2255C>G
|
|
|
ENST00000695653.1:c.1816C>G
|
ENSP00000512084.1:p.Arg606Gly
|
|
ENST00000695654.1:c.2932C>G
|
ENSP00000512085.1:p.Arg978Gly
|
|
ENST00000695690.1:n.98C>G
|
|
|
ENST00000695691.1:n.98C>G
|
|
|
ENST00000245907.11:c.3907C>G
MANE Select
|
ENSP00000245907.4:p.Arg1303Gly
|
|
ENST00000245907.10:c.3907C>G
|
ENSP00000245907.4:p.Arg1303Gly
|
|
ENST00000596238.1:n.350C>G
|
|
|
ENST00000601008.1:c.241+1696C>G
|
ENSP00000471384.1:n.241+1696C>G
|
|
NM_000064.3:c.3907C>G
|
NP_000055.2:p.Arg1303Gly
|
|
NM_000064.4:c.3907C>G
MANE Select
|
NP_000055.2:p.Arg1303Gly
|
|