|
ENST00000356839.10:c.1553G>T
MANE Select
|
ENSP00000349297.5:p.Gly518Val
|
|
|
ENST00000322910.9:c.*1508G>T
|
ENSP00000325395.5:n.*1508G>T
|
|
|
ENST00000350303.9:c.1487G>T
|
ENSP00000344152.5:p.Gly496Val
|
|
|
ENST00000356839.9:c.1553G>T
|
ENSP00000349297.5:p.Gly518Val
|
|
|
ENST00000542255.6:c.411G>T
|
|
|
|
ENST00000543245.6:c.1622G>T
|
ENSP00000438689.2:p.Gly541Val
|
|
|
ENST00000578319.5:n.48G>T
|
|
|
|
ENST00000578711.1:n.837G>T
|
|
|
|
ENST00000578809.5:n.125G>T
|
|
|
|
ENST00000579391.1:n.161G>T
|
|
|
|
ENST00000579425.5:n.669G>T
|
|
|
|
ENST00000579546.1:c.292G>T
|
|
|
|
ENST00000579894.5:n.340G>T
|
|
|
|
ENST00000582450.1:n.61G>T
|
|
|
|
ENST00000583074.5:n.174G>T
|
|
|
|
ENST00000583850.5:n.328G>T
|
|
|
|
ENST00000583858.5:c.484G>T
|
|
|
|
ENST00000585203.6:n.744G>T
|
|
|
|
NM_000018.3:c.1553G>T
|
NP_000009.1:p.Gly518Val
|
|
|
NM_001033859.2:c.1487G>T
|
NP_001029031.1:p.Gly496Val
|
|
|
NM_001270447.1:c.1622G>T
|
NP_001257376.1:p.Gly541Val
|
|
|
NM_001270448.1:c.1325G>T
|
NP_001257377.1:p.Gly442Val
|
|
|
XM_006721516.2:c.1553G>T
|
XP_006721579.2:p.Gly518Val
|
|
|
XM_011523829.1:c.1455G>T
|
XP_011522131.1:p.Arg485=
|
|
|
XM_011523830.1:c.1455G>T
|
XP_011522132.1:p.Arg485=
|
|
|
XR_934021.1:n.1660G>T
|
|
|
|
XR_934022.1:n.1562G>T
|
|
|
|
XR_934023.1:n.1562G>T
|
|
|
|
XM_006721516.3:c.1553G>T
|
XP_006721579.2:p.Gly518Val
|
|
|
XM_011523829.2:c.1455G>T
|
XP_011522131.1:p.Arg485=
|
|
|
XM_011523830.2:c.1455G>T
|
XP_011522132.1:p.Arg485=
|
|
|
XM_024450741.1:c.1455G>T
|
XP_024306509.1:p.Arg485=
|
|
|
XR_934021.2:n.1612G>T
|
|
|
|
XR_934022.2:n.1514G>T
|
|
|
|
XR_934023.2:n.1514G>T
|
|
|
|
NM_000018.4:c.1553G>T
MANE Select
|
NP_000009.1:p.Gly518Val
|
|
|
NM_001033859.3:c.1487G>T
|
NP_001029031.1:p.Gly496Val
|
|
|
NM_001270447.2:c.1622G>T
|
NP_001257376.1:p.Gly541Val
|
|
|
NM_001270448.2:c.1325G>T
|
NP_001257377.1:p.Gly442Val
|
|
