|
ENST00000356839.10:c.1634C>G
MANE Select
|
ENSP00000349297.5:p.Thr545Ser
|
|
|
ENST00000322910.9:c.*1589C>G
|
ENSP00000325395.5:n.*1589C>G
|
|
|
ENST00000350303.9:c.1568C>G
|
ENSP00000344152.5:p.Thr523Ser
|
|
|
ENST00000356839.9:c.1634C>G
|
ENSP00000349297.5:p.Thr545Ser
|
|
|
ENST00000542255.6:c.492C>G
|
|
|
|
ENST00000543245.6:c.1703C>G
|
ENSP00000438689.2:p.Thr568Ser
|
|
|
ENST00000578319.5:n.215C>G
|
|
|
|
ENST00000578711.1:n.1004C>G
|
|
|
|
ENST00000578809.5:n.206C>G
|
|
|
|
ENST00000579391.1:n.238C>G
|
|
|
|
ENST00000579425.5:n.750C>G
|
|
|
|
ENST00000579546.1:c.369C>G
|
|
|
|
ENST00000579894.5:n.421C>G
|
|
|
|
ENST00000582450.1:n.142C>G
|
|
|
|
ENST00000583074.5:n.255C>G
|
|
|
|
ENST00000583848.5:c.20C>G
|
ENSP00000466487.1:p.Thr7Ser
|
|
|
ENST00000583850.5:n.405C>G
|
|
|
|
ENST00000583858.5:c.565C>G
|
|
|
|
ENST00000585203.6:n.825C>G
|
|
|
|
NM_000018.3:c.1634C>G
|
NP_000009.1:p.Thr545Ser
|
|
|
NM_001033859.2:c.1568C>G
|
NP_001029031.1:p.Thr523Ser
|
|
|
NM_001270447.1:c.1703C>G
|
NP_001257376.1:p.Thr568Ser
|
|
|
NM_001270448.1:c.1406C>G
|
NP_001257377.1:p.Thr469Ser
|
|
|
XM_006721516.2:c.1634C>G
|
XP_006721579.2:p.Thr545Ser
|
|
|
XM_011523829.1:c.1532C>G
|
XP_011522131.1:p.Thr511Ser
|
|
|
XM_011523830.1:c.1532C>G
|
XP_011522132.1:p.Thr511Ser
|
|
|
XR_934021.1:n.1737C>G
|
|
|
|
XR_934022.1:n.1643C>G
|
|
|
|
XR_934023.1:n.1643C>G
|
|
|
|
XM_006721516.3:c.1634C>G
|
XP_006721579.2:p.Thr545Ser
|
|
|
XM_011523829.2:c.1532C>G
|
XP_011522131.1:p.Thr511Ser
|
|
|
XM_011523830.2:c.1532C>G
|
XP_011522132.1:p.Thr511Ser
|
|
|
XM_024450741.1:c.1622C>G
|
XP_024306509.1:p.Thr541Ser
|
|
|
XR_934021.2:n.1689C>G
|
|
|
|
XR_934022.2:n.1595C>G
|
|
|
|
XR_934023.2:n.1595C>G
|
|
|
|
NM_000018.4:c.1634C>G
MANE Select
|
NP_000009.1:p.Thr545Ser
|
|
|
NM_001033859.3:c.1568C>G
|
NP_001029031.1:p.Thr523Ser
|
|
|
NM_001270447.2:c.1703C>G
|
NP_001257376.1:p.Thr568Ser
|
|
|
NM_001270448.2:c.1406C>G
|
NP_001257377.1:p.Thr469Ser
|
|
