ENST00000336926.11:c.476T>C
MANE Select
|
ENSP00000336747.6:p.Phe159Ser
|
|
ENST00000336926.10:c.476T>C
|
ENSP00000336747.6:p.Phe159Ser
|
|
ENST00000420909.1:c.389T>C
|
ENSP00000414280.1:p.Phe130Ser
|
|
ENST00000434438.6:c.476T>C
|
ENSP00000410300.2:p.Phe159Ser
|
|
ENST00000616821.4:c.389T>C
|
ENSP00000484528.1:p.Phe130Ser
|
|
NM_001243198.2:c.476T>C
|
NP_001230127.1:p.Phe159Ser
|
|
NM_005338.6:c.476T>C
|
NP_005329.3:p.Phe159Ser
|
|
XM_005250304.2:c.389T>C
|
XP_005250361.1:p.Phe130Ser
|
|
XM_005250305.2:c.374T>C
|
XP_005250362.1:p.Phe125Ser
|
|
XM_011516116.1:c.476T>C
|
XP_011514418.1:p.Phe159Ser
|
|
XM_011516116.2:c.476T>C
|
XP_011514418.1:p.Phe159Ser
|
|
XM_017012099.1:c.434T>C
|
XP_016867588.1:p.Phe145Ser
|
|
NM_005338.7:c.476T>C
MANE Select
|
NP_005329.3:p.Phe159Ser
|
|
NM_001243198.3:c.476T>C
|
NP_001230127.1:p.Phe159Ser
|
|
NM_001382444.1:c.374T>C
|
NP_001369373.1:p.Phe125Ser
|
|
NM_001382445.1:c.389T>C
|
NP_001369374.1:p.Phe130Ser
|
|