|
ENST00000356839.10:c.932T>C
MANE Select
|
ENSP00000349297.5:p.Phe311Ser
|
|
|
ENST00000322910.9:c.*887T>C
|
ENSP00000325395.5:n.*887T>C
|
|
|
ENST00000350303.9:c.866T>C
|
ENSP00000344152.5:p.Phe289Ser
|
|
|
ENST00000356839.9:c.932T>C
|
ENSP00000349297.5:p.Phe311Ser
|
|
|
ENST00000543245.6:c.1001T>C
|
ENSP00000438689.2:p.Phe334Ser
|
|
|
ENST00000578824.5:n.81T>C
|
|
|
|
ENST00000581378.5:c.650T>C
|
|
|
|
ENST00000582379.1:n.316T>C
|
|
|
|
NM_000018.3:c.932T>C
|
NP_000009.1:p.Phe311Ser
|
|
|
NM_001033859.2:c.866T>C
|
NP_001029031.1:p.Phe289Ser
|
|
|
NM_001270447.1:c.1001T>C
|
NP_001257376.1:p.Phe334Ser
|
|
|
NM_001270448.1:c.704T>C
|
NP_001257377.1:p.Phe235Ser
|
|
|
XM_006721516.2:c.932T>C
|
XP_006721579.2:p.Phe311Ser
|
|
|
XM_011523829.1:c.932T>C
|
XP_011522131.1:p.Phe311Ser
|
|
|
XM_011523830.1:c.932T>C
|
XP_011522132.1:p.Phe311Ser
|
|
|
XR_934021.1:n.1039T>C
|
|
|
|
XR_934022.1:n.1039T>C
|
|
|
|
XR_934023.1:n.1039T>C
|
|
|
|
XM_006721516.3:c.932T>C
|
XP_006721579.2:p.Phe311Ser
|
|
|
XM_011523829.2:c.932T>C
|
XP_011522131.1:p.Phe311Ser
|
|
|
XM_011523830.2:c.932T>C
|
XP_011522132.1:p.Phe311Ser
|
|
|
XM_024450741.1:c.932T>C
|
XP_024306509.1:p.Phe311Ser
|
|
|
XR_934021.2:n.991T>C
|
|
|
|
XR_934022.2:n.991T>C
|
|
|
|
XR_934023.2:n.991T>C
|
|
|
|
NM_000018.4:c.932T>C
MANE Select
|
NP_000009.1:p.Phe311Ser
|
|
|
NM_001033859.3:c.866T>C
|
NP_001029031.1:p.Phe289Ser
|
|
|
NM_001270447.2:c.1001T>C
|
NP_001257376.1:p.Phe334Ser
|
|
|
NM_001270448.2:c.704T>C
|
NP_001257377.1:p.Phe235Ser
|
|
