ENST00000356839.10:c.1861C>G
MANE Select
|
ENSP00000349297.5:p.Leu621Val
|
|
ENST00000322910.9:c.*1816C>G
|
ENSP00000325395.5:n.*1816C>G
|
|
ENST00000350303.9:c.1795C>G
|
ENSP00000344152.5:p.Leu599Val
|
|
ENST00000356839.9:c.1861C>G
|
ENSP00000349297.5:p.Leu621Val
|
|
ENST00000542255.6:c.740C>G
|
|
|
ENST00000543245.6:c.1930C>G
|
ENSP00000438689.2:p.Leu644Val
|
|
ENST00000578033.1:n.286C>G
|
|
|
ENST00000578319.5:n.442C>G
|
|
|
ENST00000578711.1:n.1486C>G
|
|
|
ENST00000578809.5:n.433C>G
|
|
|
ENST00000579425.5:n.977C>G
|
|
|
ENST00000583848.5:c.227C>G
|
ENSP00000466487.1:n.227C>G
|
|
ENST00000583850.5:n.632C>G
|
|
|
ENST00000583858.5:c.792C>G
|
|
|
NM_000018.3:c.1861C>G
|
NP_000009.1:p.Leu621Val
|
|
NM_001033859.2:c.1795C>G
|
NP_001029031.1:p.Leu599Val
|
|
NM_001270447.1:c.1930C>G
|
NP_001257376.1:p.Leu644Val
|
|
NM_001270448.1:c.1633C>G
|
NP_001257377.1:p.Leu545Val
|
|
XM_006721516.2:c.1882C>G
|
XP_006721579.2:p.Leu628Val
|
|
XM_011523829.1:c.1780C>G
|
XP_011522131.1:p.Leu594Val
|
|
XM_011523830.1:c.1759C>G
|
XP_011522132.1:p.Leu587Val
|
|
XR_934021.1:n.1964C>G
|
|
|
XR_934022.1:n.1870C>G
|
|
|
XR_934023.1:n.1891C>G
|
|
|
XM_006721516.3:c.1882C>G
|
XP_006721579.2:p.Leu628Val
|
|
XM_011523829.2:c.1780C>G
|
XP_011522131.1:p.Leu594Val
|
|
XM_011523830.2:c.1759C>G
|
XP_011522132.1:p.Leu587Val
|
|
XM_024450741.1:c.1849C>G
|
XP_024306509.1:p.Leu617Val
|
|
XR_934021.2:n.1916C>G
|
|
|
XR_934022.2:n.1822C>G
|
|
|
XR_934023.2:n.1843C>G
|
|
|
NM_000018.4:c.1861C>G
MANE Select
|
NP_000009.1:p.Leu621Val
|
|
NM_001033859.3:c.1795C>G
|
NP_001029031.1:p.Leu599Val
|
|
NM_001270447.2:c.1930C>G
|
NP_001257376.1:p.Leu644Val
|
|
NM_001270448.2:c.1633C>G
|
NP_001257377.1:p.Leu545Val
|
|