|
ENST00000356839.10:c.1645G>A
MANE Select
|
ENSP00000349297.5:p.Ala549Thr
|
|
|
ENST00000322910.9:c.*1600G>A
|
ENSP00000325395.5:n.*1600G>A
|
|
|
ENST00000350303.9:c.1579G>A
|
ENSP00000344152.5:p.Ala527Thr
|
|
|
ENST00000356839.9:c.1645G>A
|
ENSP00000349297.5:p.Ala549Thr
|
|
|
ENST00000542255.6:c.503G>A
|
|
|
|
ENST00000543245.6:c.1714G>A
|
ENSP00000438689.2:p.Ala572Thr
|
|
|
ENST00000578319.5:n.226G>A
|
|
|
|
ENST00000578711.1:n.1015G>A
|
|
|
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ENST00000578809.5:n.217G>A
|
|
|
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ENST00000579391.1:n.249G>A
|
|
|
|
ENST00000579425.5:n.761G>A
|
|
|
|
ENST00000579546.1:c.380G>A
|
|
|
|
ENST00000582450.1:n.153G>A
|
|
|
|
ENST00000583074.5:n.266G>A
|
|
|
|
ENST00000583848.5:c.31G>A
|
ENSP00000466487.1:p.Ala11Thr
|
|
|
ENST00000583850.5:n.416G>A
|
|
|
|
ENST00000583858.5:c.576G>A
|
|
|
|
ENST00000585203.6:n.836G>A
|
|
|
|
NM_000018.3:c.1645G>A
|
NP_000009.1:p.Ala549Thr
|
|
|
NM_001033859.2:c.1579G>A
|
NP_001029031.1:p.Ala527Thr
|
|
|
NM_001270447.1:c.1714G>A
|
NP_001257376.1:p.Ala572Thr
|
|
|
NM_001270448.1:c.1417G>A
|
NP_001257377.1:p.Ala473Thr
|
|
|
XM_006721516.2:c.1645G>A
|
XP_006721579.2:p.Ala549Thr
|
|
|
XM_011523829.1:c.1543G>A
|
XP_011522131.1:p.Ala515Thr
|
|
|
XM_011523830.1:c.1543G>A
|
XP_011522132.1:p.Ala515Thr
|
|
|
XR_934021.1:n.1748G>A
|
|
|
|
XR_934022.1:n.1654G>A
|
|
|
|
XR_934023.1:n.1654G>A
|
|
|
|
XM_006721516.3:c.1645G>A
|
XP_006721579.2:p.Ala549Thr
|
|
|
XM_011523829.2:c.1543G>A
|
XP_011522131.1:p.Ala515Thr
|
|
|
XM_011523830.2:c.1543G>A
|
XP_011522132.1:p.Ala515Thr
|
|
|
XM_024450741.1:c.1633G>A
|
XP_024306509.1:p.Ala545Thr
|
|
|
XR_934021.2:n.1700G>A
|
|
|
|
XR_934022.2:n.1606G>A
|
|
|
|
XR_934023.2:n.1606G>A
|
|
|
|
NM_000018.4:c.1645G>A
MANE Select
|
NP_000009.1:p.Ala549Thr
|
|
|
NM_001033859.3:c.1579G>A
|
NP_001029031.1:p.Ala527Thr
|
|
|
NM_001270447.2:c.1714G>A
|
NP_001257376.1:p.Ala572Thr
|
|
|
NM_001270448.2:c.1417G>A
|
NP_001257377.1:p.Ala473Thr
|
|
