ENST00000695651.1:n.2612G>T
|
|
|
ENST00000695653.1:c.2173G>T
|
ENSP00000512084.1:p.Ala725Ser
|
|
ENST00000695654.1:c.3289G>T
|
ENSP00000512085.1:p.Ala1097Ser
|
|
ENST00000695689.1:c.235G>T
|
ENSP00000512101.1:n.235G>T
|
|
ENST00000695690.1:n.455G>T
|
|
|
ENST00000695691.1:n.455G>T
|
|
|
ENST00000245907.11:c.4264G>T
MANE Select
|
ENSP00000245907.4:p.Ala1422Ser
|
|
ENST00000245907.10:c.4264G>T
|
ENSP00000245907.4:p.Ala1422Ser
|
|
ENST00000596548.1:c.385G>T
|
ENSP00000469744.1:p.Ala129Ser
|
|
ENST00000599899.5:n.1223G>T
|
|
|
ENST00000601008.1:c.242-4069G>T
|
ENSP00000471384.1:n.242-4069G>T
|
|
NM_000064.3:c.4264G>T
|
NP_000055.2:p.Ala1422Ser
|
|
NM_000064.4:c.4264G>T
MANE Select
|
NP_000055.2:p.Ala1422Ser
|
|