ENST00000695651.1:n.1051G>C
|
|
|
ENST00000695652.1:c.2580G>C
|
ENSP00000512083.1:p.Val860=
|
|
ENST00000695653.1:c.612G>C
|
ENSP00000512084.1:p.Val204=
|
|
ENST00000695654.1:c.1827G>C
|
ENSP00000512085.1:p.Val609=
|
|
ENST00000695655.1:c.1644G>C
|
ENSP00000512086.1:n.1644G>C
|
|
ENST00000695692.1:n.2067G>C
|
|
|
ENST00000245907.11:c.2703G>C
MANE Select
|
ENSP00000245907.4:p.Val901=
|
|
ENST00000245907.10:c.2703G>C
|
ENSP00000245907.4:p.Val901=
|
|
ENST00000594005.1:n.279G>C
|
|
|
NM_000064.3:c.2703G>C
|
NP_000055.2:p.Val901=
|
|
NM_000064.4:c.2703G>C
MANE Select
|
NP_000055.2:p.Val901=
|
|