|
ENST00000356839.10:c.1595G>C
MANE Select
|
ENSP00000349297.5:p.Ser532Thr
|
|
|
ENST00000322910.9:c.*1550G>C
|
ENSP00000325395.5:n.*1550G>C
|
|
|
ENST00000350303.9:c.1529G>C
|
ENSP00000344152.5:p.Ser510Thr
|
|
|
ENST00000356839.9:c.1595G>C
|
ENSP00000349297.5:p.Ser532Thr
|
|
|
ENST00000542255.6:c.453G>C
|
|
|
|
ENST00000543245.6:c.1664G>C
|
ENSP00000438689.2:p.Ser555Thr
|
|
|
ENST00000578319.5:n.90G>C
|
|
|
|
ENST00000578711.1:n.879G>C
|
|
|
|
ENST00000578809.5:n.167G>C
|
|
|
|
ENST00000579391.1:n.203G>C
|
|
|
|
ENST00000579425.5:n.711G>C
|
|
|
|
ENST00000579546.1:c.334G>C
|
|
|
|
ENST00000579894.5:n.382G>C
|
|
|
|
ENST00000582450.1:n.103G>C
|
|
|
|
ENST00000583074.5:n.216G>C
|
|
|
|
ENST00000583850.5:n.370G>C
|
|
|
|
ENST00000583858.5:c.526G>C
|
|
|
|
ENST00000585203.6:n.786G>C
|
|
|
|
NM_000018.3:c.1595G>C
|
NP_000009.1:p.Ser532Thr
|
|
|
NM_001033859.2:c.1529G>C
|
NP_001029031.1:p.Ser510Thr
|
|
|
NM_001270447.1:c.1664G>C
|
NP_001257376.1:p.Ser555Thr
|
|
|
NM_001270448.1:c.1367G>C
|
NP_001257377.1:p.Ser456Thr
|
|
|
XM_006721516.2:c.1595G>C
|
XP_006721579.2:p.Ser532Thr
|
|
|
XM_011523829.1:c.1497G>C
|
XP_011522131.1:p.Glu499Asp
|
|
|
XM_011523830.1:c.1497G>C
|
XP_011522132.1:p.Glu499Asp
|
|
|
XR_934021.1:n.1702G>C
|
|
|
|
XR_934022.1:n.1604G>C
|
|
|
|
XR_934023.1:n.1604G>C
|
|
|
|
XM_006721516.3:c.1595G>C
|
XP_006721579.2:p.Ser532Thr
|
|
|
XM_011523829.2:c.1497G>C
|
XP_011522131.1:p.Glu499Asp
|
|
|
XM_011523830.2:c.1497G>C
|
XP_011522132.1:p.Glu499Asp
|
|
|
XM_024450741.1:c.1497G>C
|
XP_024306509.1:p.Glu499Asp
|
|
|
XR_934021.2:n.1654G>C
|
|
|
|
XR_934022.2:n.1556G>C
|
|
|
|
XR_934023.2:n.1556G>C
|
|
|
|
NM_000018.4:c.1595G>C
MANE Select
|
NP_000009.1:p.Ser532Thr
|
|
|
NM_001033859.3:c.1529G>C
|
NP_001029031.1:p.Ser510Thr
|
|
|
NM_001270447.2:c.1664G>C
|
NP_001257376.1:p.Ser555Thr
|
|
|
NM_001270448.2:c.1367G>C
|
NP_001257377.1:p.Ser456Thr
|
|
