ENST00000695651.1:n.2176C>T
|
|
|
ENST00000695653.1:c.1737C>T
|
ENSP00000512084.1:p.Phe579=
|
|
ENST00000695654.1:c.2853C>T
|
ENSP00000512085.1:p.Phe951=
|
|
ENST00000695690.1:n.19C>T
|
|
|
ENST00000695691.1:n.19C>T
|
|
|
ENST00000245907.11:c.3828C>T
MANE Select
|
ENSP00000245907.4:p.Phe1276=
|
|
ENST00000245907.10:c.3828C>T
|
ENSP00000245907.4:p.Phe1276=
|
|
ENST00000596238.1:n.271C>T
|
|
|
ENST00000601008.1:c.241+1617C>T
|
ENSP00000471384.1:n.241+1617C>T
|
|
NM_000064.3:c.3828C>T
|
NP_000055.2:p.Phe1276=
|
|
NM_000064.4:c.3828C>T
MANE Select
|
NP_000055.2:p.Phe1276=
|
|