|
ENST00000356839.10:c.1597G>T
MANE Select
|
ENSP00000349297.5:p.Gly533Cys
|
|
|
ENST00000322910.9:c.*1552G>T
|
ENSP00000325395.5:n.*1552G>T
|
|
|
ENST00000350303.9:c.1531G>T
|
ENSP00000344152.5:p.Gly511Cys
|
|
|
ENST00000356839.9:c.1597G>T
|
ENSP00000349297.5:p.Gly533Cys
|
|
|
ENST00000542255.6:c.455G>T
|
|
|
|
ENST00000543245.6:c.1666G>T
|
ENSP00000438689.2:p.Gly556Cys
|
|
|
ENST00000578319.5:n.92G>T
|
|
|
|
ENST00000578711.1:n.881G>T
|
|
|
|
ENST00000578809.5:n.169G>T
|
|
|
|
ENST00000579391.1:n.205G>T
|
|
|
|
ENST00000579425.5:n.713G>T
|
|
|
|
ENST00000579546.1:c.336G>T
|
|
|
|
ENST00000579894.5:n.384G>T
|
|
|
|
ENST00000582450.1:n.105G>T
|
|
|
|
ENST00000583074.5:n.218G>T
|
|
|
|
ENST00000583850.5:n.372G>T
|
|
|
|
ENST00000583858.5:c.528G>T
|
|
|
|
ENST00000585203.6:n.788G>T
|
|
|
|
NM_000018.3:c.1597G>T
|
NP_000009.1:p.Gly533Cys
|
|
|
NM_001033859.2:c.1531G>T
|
NP_001029031.1:p.Gly511Cys
|
|
|
NM_001270447.1:c.1666G>T
|
NP_001257376.1:p.Gly556Cys
|
|
|
NM_001270448.1:c.1369G>T
|
NP_001257377.1:p.Gly457Cys
|
|
|
XM_006721516.2:c.1597G>T
|
XP_006721579.2:p.Gly533Cys
|
|
|
XM_011523829.1:c.1499G>T
|
XP_011522131.1:p.Trp500Leu
|
|
|
XM_011523830.1:c.1499G>T
|
XP_011522132.1:p.Trp500Leu
|
|
|
XR_934021.1:n.1704G>T
|
|
|
|
XR_934022.1:n.1606G>T
|
|
|
|
XR_934023.1:n.1606G>T
|
|
|
|
XM_006721516.3:c.1597G>T
|
XP_006721579.2:p.Gly533Cys
|
|
|
XM_011523829.2:c.1499G>T
|
XP_011522131.1:p.Trp500Leu
|
|
|
XM_011523830.2:c.1499G>T
|
XP_011522132.1:p.Trp500Leu
|
|
|
XM_024450741.1:c.1499G>T
|
XP_024306509.1:p.Trp500Leu
|
|
|
XR_934021.2:n.1656G>T
|
|
|
|
XR_934022.2:n.1558G>T
|
|
|
|
XR_934023.2:n.1558G>T
|
|
|
|
NM_000018.4:c.1597G>T
MANE Select
|
NP_000009.1:p.Gly533Cys
|
|
|
NM_001033859.3:c.1531G>T
|
NP_001029031.1:p.Gly511Cys
|
|
|
NM_001270447.2:c.1666G>T
|
NP_001257376.1:p.Gly556Cys
|
|
|
NM_001270448.2:c.1369G>T
|
NP_001257377.1:p.Gly457Cys
|
|
