ENST00000695651.1:n.2523A>C
|
|
|
ENST00000695653.1:c.2084A>C
|
ENSP00000512084.1:p.Tyr695Ser
|
|
ENST00000695654.1:c.3200A>C
|
ENSP00000512085.1:p.Tyr1067Ser
|
|
ENST00000695689.1:c.146A>C
|
ENSP00000512101.1:n.146A>C
|
|
ENST00000695690.1:n.366A>C
|
|
|
ENST00000695691.1:n.366A>C
|
|
|
ENST00000245907.11:c.4175A>C
MANE Select
|
ENSP00000245907.4:p.Tyr1392Ser
|
|
ENST00000245907.10:c.4175A>C
|
ENSP00000245907.4:p.Tyr1392Ser
|
|
ENST00000596548.1:c.296A>C
|
ENSP00000469744.1:p.Tyr99Ser
|
|
ENST00000599899.5:n.1134A>C
|
|
|
ENST00000601008.1:c.242-4269A>C
|
ENSP00000471384.1:n.242-4269A>C
|
|
NM_000064.3:c.4175A>C
|
NP_000055.2:p.Tyr1392Ser
|
|
NM_000064.4:c.4175A>C
MANE Select
|
NP_000055.2:p.Tyr1392Ser
|
|