|
ENST00000356839.10:c.1600G>T
MANE Select
|
ENSP00000349297.5:p.Glu534Ter
|
|
|
ENST00000322910.9:c.*1555G>T
|
ENSP00000325395.5:n.*1555G>T
|
|
|
ENST00000350303.9:c.1534G>T
|
ENSP00000344152.5:p.Glu512Ter
|
|
|
ENST00000356839.9:c.1600G>T
|
ENSP00000349297.5:p.Glu534Ter
|
|
|
ENST00000542255.6:c.458G>T
|
|
|
|
ENST00000543245.6:c.1669G>T
|
ENSP00000438689.2:p.Glu557Ter
|
|
|
ENST00000578319.5:n.95G>T
|
|
|
|
ENST00000578711.1:n.884G>T
|
|
|
|
ENST00000578809.5:n.172G>T
|
|
|
|
ENST00000579391.1:n.208G>T
|
|
|
|
ENST00000579425.5:n.716G>T
|
|
|
|
ENST00000579546.1:c.339G>T
|
|
|
|
ENST00000579894.5:n.387G>T
|
|
|
|
ENST00000582450.1:n.108G>T
|
|
|
|
ENST00000583074.5:n.221G>T
|
|
|
|
ENST00000583850.5:n.375G>T
|
|
|
|
ENST00000583858.5:c.531G>T
|
|
|
|
ENST00000585203.6:n.791G>T
|
|
|
|
NM_000018.3:c.1600G>T
|
NP_000009.1:p.Glu534Ter
|
|
|
NM_001033859.2:c.1534G>T
|
NP_001029031.1:p.Glu512Ter
|
|
|
NM_001270447.1:c.1669G>T
|
NP_001257376.1:p.Glu557Ter
|
|
|
NM_001270448.1:c.1372G>T
|
NP_001257377.1:p.Glu458Ter
|
|
|
XM_006721516.2:c.1600G>T
|
XP_006721579.2:p.Glu534Ter
|
|
|
XM_011523829.1:c.1502G>T
|
XP_011522131.1:p.Arg501Leu
|
|
|
XM_011523830.1:c.1502G>T
|
XP_011522132.1:p.Arg501Leu
|
|
|
XR_934021.1:n.1707G>T
|
|
|
|
XR_934022.1:n.1609G>T
|
|
|
|
XR_934023.1:n.1609G>T
|
|
|
|
XM_006721516.3:c.1600G>T
|
XP_006721579.2:p.Glu534Ter
|
|
|
XM_011523829.2:c.1502G>T
|
XP_011522131.1:p.Arg501Leu
|
|
|
XM_011523830.2:c.1502G>T
|
XP_011522132.1:p.Arg501Leu
|
|
|
XM_024450741.1:c.1502G>T
|
XP_024306509.1:p.Arg501Leu
|
|
|
XR_934021.2:n.1659G>T
|
|
|
|
XR_934022.2:n.1561G>T
|
|
|
|
XR_934023.2:n.1561G>T
|
|
|
|
NM_000018.4:c.1600G>T
MANE Select
|
NP_000009.1:p.Glu534Ter
|
|
|
NM_001033859.3:c.1534G>T
|
NP_001029031.1:p.Glu512Ter
|
|
|
NM_001270447.2:c.1669G>T
|
NP_001257376.1:p.Glu557Ter
|
|
|
NM_001270448.2:c.1372G>T
|
NP_001257377.1:p.Glu458Ter
|
|
