ENST00000318471.5:c.191T>C
MANE Select
|
ENSP00000315680.3:p.Phe64Ser
|
|
ENST00000541292.6:c.191T>C
|
ENSP00000441004.1:p.Phe64Ser
|
|
ENST00000678002.1:c.66T>C
|
|
|
ENST00000678557.1:c.77T>C
|
ENSP00000502962.1:p.Phe26Ser
|
|
ENST00000678593.1:c.196T>C
|
ENSP00000503841.1:p.Leu66=
|
|
ENST00000679286.1:c.71T>C
|
ENSP00000503168.1:p.Phe24Ser
|
|
ENST00000318471.4:c.191T>C
|
ENSP00000315680.3:p.Phe64Ser
|
|
ENST00000367756.8:c.191T>C
|
ENSP00000356730.4:p.Phe64Ser
|
|
ENST00000541292.5:c.191T>C
|
ENSP00000441004.1:p.Phe64Ser
|
|
NM_000288.3:c.191T>C
|
NP_000279.1:p.Phe64Ser
|
|
XM_005267019.3:c.77T>C
|
XP_005267076.1:p.Phe26Ser
|
|
XM_006715502.1:c.191T>C
|
XP_006715565.1:p.Phe64Ser
|
|
XM_011535900.1:c.191T>C
|
XP_011534202.1:p.Phe64Ser
|
|
XM_005267019.4:c.77T>C
|
XP_005267076.1:p.Phe26Ser
|
|
XM_006715502.2:c.191T>C
|
XP_006715565.1:p.Phe64Ser
|
|
XM_017010934.2:c.191T>C
|
XP_016866423.1:p.Phe64Ser
|
|
NM_000288.4:c.191T>C
MANE Select
|
NP_000279.1:p.Phe64Ser
|
|