|
ENST00000356839.10:c.1226C=
MANE Select
|
ENSP00000349297.5:p.Thr409=
|
|
|
ENST00000322910.9:c.*1181C=
|
ENSP00000325395.5:n.*1181C=
|
|
|
ENST00000350303.9:c.1160C=
|
ENSP00000344152.5:p.Thr387=
|
|
|
ENST00000356839.9:c.1226C=
|
ENSP00000349297.5:p.Thr409=
|
|
|
ENST00000542255.6:c.84C=
|
|
|
|
ENST00000543245.6:c.1295C=
|
ENSP00000438689.2:p.Thr432=
|
|
|
ENST00000578579.2:n.397C=
|
|
|
|
ENST00000578711.1:n.183C=
|
|
|
|
ENST00000578824.5:n.642C=
|
|
|
|
ENST00000579425.5:n.250C=
|
|
|
|
ENST00000579546.1:c.63C=
|
|
|
|
ENST00000583850.5:n.1C=
|
|
|
|
ENST00000583858.5:c.255C=
|
|
|
|
ENST00000585203.6:n.434C=
|
|
|
|
NM_000018.3:c.1226C=
|
NP_000009.1:p.Thr409=
|
|
|
NM_001033859.2:c.1160C=
|
NP_001029031.1:p.Thr387=
|
|
|
NM_001270447.1:c.1295C=
|
NP_001257376.1:p.Thr432=
|
|
|
NM_001270448.1:c.998C=
|
NP_001257377.1:p.Thr333=
|
|
|
XM_006721516.2:c.1226C=
|
XP_006721579.2:p.Thr409=
|
|
|
XM_011523829.1:c.1226C=
|
XP_011522131.1:p.Thr409=
|
|
|
XM_011523830.1:c.1226C=
|
XP_011522132.1:p.Thr409=
|
|
|
XR_934021.1:n.1333C=
|
|
|
|
XR_934022.1:n.1333C=
|
|
|
|
XR_934023.1:n.1333C=
|
|
|
|
XM_006721516.3:c.1226C=
|
XP_006721579.2:p.Thr409=
|
|
|
XM_011523829.2:c.1226C=
|
XP_011522131.1:p.Thr409=
|
|
|
XM_011523830.2:c.1226C=
|
XP_011522132.1:p.Thr409=
|
|
|
XM_024450741.1:c.1226C=
|
XP_024306509.1:p.Thr409=
|
|
|
XR_934021.2:n.1285C=
|
|
|
|
XR_934022.2:n.1285C=
|
|
|
|
XR_934023.2:n.1285C=
|
|
|
|
NM_000018.4:c.1226C=
MANE Select
|
NP_000009.1:p.Thr409=
|
|
|
NM_001033859.3:c.1160C=
|
NP_001029031.1:p.Thr387=
|
|
|
NM_001270447.2:c.1295C=
|
NP_001257376.1:p.Thr432=
|
|
|
NM_001270448.2:c.998C=
|
NP_001257377.1:p.Thr333=
|
|
