ENST00000356839.10:c.1891T>G
MANE Select
|
ENSP00000349297.5:p.Tyr631Asp
|
|
ENST00000322910.9:c.*1846T>G
|
ENSP00000325395.5:n.*1846T>G
|
|
ENST00000350303.9:c.1825T>G
|
ENSP00000344152.5:p.Tyr609Asp
|
|
ENST00000356839.9:c.1891T>G
|
ENSP00000349297.5:p.Tyr631Asp
|
|
ENST00000542255.6:c.770T>G
|
|
|
ENST00000543245.6:c.1960T>G
|
ENSP00000438689.2:p.Tyr654Asp
|
|
ENST00000578033.1:n.316T>G
|
|
|
ENST00000578319.5:n.472T>G
|
|
|
ENST00000578711.1:n.1516T>G
|
|
|
ENST00000578809.5:n.463T>G
|
|
|
ENST00000579425.5:n.1007T>G
|
|
|
ENST00000583848.5:c.257T>G
|
ENSP00000466487.1:n.257T>G
|
|
ENST00000583850.5:n.662T>G
|
|
|
ENST00000583858.5:c.822T>G
|
|
|
NM_000018.3:c.1891T>G
|
NP_000009.1:p.Tyr631Asp
|
|
NM_001033859.2:c.1825T>G
|
NP_001029031.1:p.Tyr609Asp
|
|
NM_001270447.1:c.1960T>G
|
NP_001257376.1:p.Tyr654Asp
|
|
NM_001270448.1:c.1663T>G
|
NP_001257377.1:p.Tyr555Asp
|
|
XM_006721516.2:c.1912T>G
|
XP_006721579.2:p.Tyr638Asp
|
|
XM_011523829.1:c.1810T>G
|
XP_011522131.1:p.Tyr604Asp
|
|
XM_011523830.1:c.1789T>G
|
XP_011522132.1:p.Tyr597Asp
|
|
XR_934021.1:n.1994T>G
|
|
|
XR_934022.1:n.1900T>G
|
|
|
XR_934023.1:n.1921T>G
|
|
|
XM_006721516.3:c.1912T>G
|
XP_006721579.2:p.Tyr638Asp
|
|
XM_011523829.2:c.1810T>G
|
XP_011522131.1:p.Tyr604Asp
|
|
XM_011523830.2:c.1789T>G
|
XP_011522132.1:p.Tyr597Asp
|
|
XM_024450741.1:c.1879T>G
|
XP_024306509.1:p.Tyr627Asp
|
|
XR_934021.2:n.1946T>G
|
|
|
XR_934022.2:n.1852T>G
|
|
|
XR_934023.2:n.1873T>G
|
|
|
NM_000018.4:c.1891T>G
MANE Select
|
NP_000009.1:p.Tyr631Asp
|
|
NM_001033859.3:c.1825T>G
|
NP_001029031.1:p.Tyr609Asp
|
|
NM_001270447.2:c.1960T>G
|
NP_001257376.1:p.Tyr654Asp
|
|
NM_001270448.2:c.1663T>G
|
NP_001257377.1:p.Tyr555Asp
|
|