ENST00000508233.6:c.421C>T
|
ENSP00000422973.2:p.Pro141Ser
|
|
ENST00000614857.5:c.544C>T
|
ENSP00000477824.2:p.Pro182Ser
|
|
ENST00000681973.1:n.771C>T
|
|
|
ENST00000682026.1:n.497C>T
|
|
|
ENST00000682448.1:n.2030C>T
|
|
|
ENST00000682554.1:n.1992C>T
|
|
|
ENST00000682599.1:n.3032C>T
|
|
|
ENST00000682627.1:n.464C>T
|
|
|
ENST00000682865.1:n.828C>T
|
|
|
ENST00000683087.1:n.558C>T
|
|
|
ENST00000683168.1:n.1298C>T
|
|
|
ENST00000683620.1:n.1726C>T
|
|
|
ENST00000684106.1:n.2794C>T
|
|
|
ENST00000684450.1:n.1603C>T
|
|
|
ENST00000684710.1:n.1835C>T
|
|
|
ENST00000395080.8:c.544C>T
MANE Select
|
ENSP00000378517.3:p.Pro182Ser
|
|
ENST00000237623.11:c.502C>T
|
ENSP00000237623.7:p.Pro168Ser
|
|
ENST00000360804.4:c.463C>T
|
ENSP00000354042.4:p.Pro155Ser
|
|
ENST00000395080.7:c.544C>T
|
ENSP00000378517.3:p.Pro182Ser
|
|
ENST00000508233.5:c.421C>T
|
ENSP00000422973.1:p.Pro141Ser
|
|
ENST00000509659.5:n.833C>T
|
|
|
ENST00000614857.4:c.478C>T
|
ENSP00000477824.1:p.Pro160Ser
|
|
NM_000582.2:c.502C>T
|
NP_000573.1:p.Pro168Ser
|
|
NM_001040058.1:c.544C>T
|
NP_001035147.1:p.Pro182Ser
|
|
NM_001040060.1:c.463C>T
|
NP_001035149.1:p.Pro155Ser
|
|
NM_001251829.1:c.421C>T
|
NP_001238758.1:p.Pro141Ser
|
|
NM_001251830.1:c.583C>T
|
NP_001238759.1:p.Pro195Ser
|
|
NM_001040058.2:c.544C>T
MANE Select
|
NP_001035147.1:p.Pro182Ser
|
|
NM_000582.3:c.502C>T
|
NP_000573.1:p.Pro168Ser
|
|
NM_001040060.2:c.463C>T
|
NP_001035149.1:p.Pro155Ser
|
|
NM_001251829.2:c.421C>T
|
NP_001238758.1:p.Pro141Ser
|
|
NM_001251830.2:c.583C>T
|
NP_001238759.1:p.Pro195Ser
|
|