ENST00000695651.1:n.2286G>C
|
|
|
ENST00000695653.1:c.1847G>C
|
ENSP00000512084.1:p.Trp616Ser
|
|
ENST00000695654.1:c.2963G>C
|
ENSP00000512085.1:p.Trp988Ser
|
|
ENST00000695690.1:n.129G>C
|
|
|
ENST00000695691.1:n.129G>C
|
|
|
ENST00000245907.11:c.3938G>C
MANE Select
|
ENSP00000245907.4:p.Trp1313Ser
|
|
ENST00000245907.10:c.3938G>C
|
ENSP00000245907.4:p.Trp1313Ser
|
|
ENST00000596238.1:n.381G>C
|
|
|
ENST00000596548.1:c.20G>C
|
ENSP00000469744.1:p.Trp7Ser
|
|
ENST00000601008.1:c.241+1727G>C
|
ENSP00000471384.1:n.241+1727G>C
|
|
NM_000064.3:c.3938G>C
|
NP_000055.2:p.Trp1313Ser
|
|
NM_000064.4:c.3938G>C
MANE Select
|
NP_000055.2:p.Trp1313Ser
|
|