ENST00000247933.9:c.1723T>G
|
ENSP00000247933.4:p.Ser575Ala
|
|
ENST00000514224.2:c.1723T>G
MANE Select
|
ENSP00000425081.2:p.Ser575Ala
|
|
ENST00000652070.1:n.1779T>G
|
|
|
ENST00000247933.8:c.1723T>G
|
ENSP00000247933.4:p.Ser575Ala
|
|
ENST00000514224.1:c.1327T>G
|
ENSP00000425081.1:p.Ser443Ala
|
|
ENST00000514417.1:n.115T>G
|
|
|
ENST00000514698.5:n.1830T>G
|
|
|
NM_000203.4:c.1723T>G
|
NP_000194.2:p.Ser575Ala
|
|
NR_110313.1:n.1811T>G
|
|
|
XM_006713882.2:c.1327T>G
|
XP_006713945.1:p.Ser443Ala
|
|
XM_011513459.1:c.1789T>G
|
XP_011511761.1:p.Ser597Ala
|
|
XM_011513460.1:c.1582T>G
|
XP_011511762.1:p.Ser528Ala
|
|
XM_011513461.1:c.1516T>G
|
XP_011511763.1:p.Ser506Ala
|
|
XM_011513462.1:c.1435T>G
|
XP_011511764.1:p.Ser479Ala
|
|
XM_011513463.1:c.1435T>G
|
XP_011511765.1:p.Ser479Ala
|
|
XR_924947.1:n.1979T>G
|
|
|
NM_000203.5:c.1723T>G
MANE Select
|
NP_000194.2:p.Ser575Ala
|
|
NM_001363576.1:c.1327T>G
|
NP_001350505.1:p.Ser443Ala
|
|
XM_011513461.2:c.1516T>G
|
XP_011511763.1:p.Ser506Ala
|
|
XM_017008163.1:c.763T>G
|
XP_016863652.1:p.Ser255Ala
|
|