ENST00000356839.10:c.1841T>G
MANE Select
|
ENSP00000349297.5:p.Ile614Ser
|
|
ENST00000322910.9:c.*1796T>G
|
ENSP00000325395.5:n.*1796T>G
|
|
ENST00000350303.9:c.1775T>G
|
ENSP00000344152.5:p.Ile592Ser
|
|
ENST00000356839.9:c.1841T>G
|
ENSP00000349297.5:p.Ile614Ser
|
|
ENST00000542255.6:c.720T>G
|
|
|
ENST00000543245.6:c.1910T>G
|
ENSP00000438689.2:p.Ile637Ser
|
|
ENST00000578033.1:n.266T>G
|
|
|
ENST00000578319.5:n.422T>G
|
|
|
ENST00000578711.1:n.1466T>G
|
|
|
ENST00000578809.5:n.413T>G
|
|
|
ENST00000579425.5:n.957T>G
|
|
|
ENST00000579546.1:c.576T>G
|
|
|
ENST00000583848.5:c.207T>G
|
ENSP00000466487.1:n.207T>G
|
|
ENST00000583850.5:n.612T>G
|
|
|
ENST00000583858.5:c.772T>G
|
|
|
NM_000018.3:c.1841T>G
|
NP_000009.1:p.Ile614Ser
|
|
NM_001033859.2:c.1775T>G
|
NP_001029031.1:p.Ile592Ser
|
|
NM_001270447.1:c.1910T>G
|
NP_001257376.1:p.Ile637Ser
|
|
NM_001270448.1:c.1613T>G
|
NP_001257377.1:p.Ile538Ser
|
|
XM_006721516.2:c.1862T>G
|
XP_006721579.2:p.Ile621Ser
|
|
XM_011523829.1:c.1760T>G
|
XP_011522131.1:p.Ile587Ser
|
|
XM_011523830.1:c.1739T>G
|
XP_011522132.1:p.Ile580Ser
|
|
XR_934021.1:n.1944T>G
|
|
|
XR_934022.1:n.1850T>G
|
|
|
XR_934023.1:n.1871T>G
|
|
|
XM_006721516.3:c.1862T>G
|
XP_006721579.2:p.Ile621Ser
|
|
XM_011523829.2:c.1760T>G
|
XP_011522131.1:p.Ile587Ser
|
|
XM_011523830.2:c.1739T>G
|
XP_011522132.1:p.Ile580Ser
|
|
XM_024450741.1:c.1829T>G
|
XP_024306509.1:p.Ile610Ser
|
|
XR_934021.2:n.1896T>G
|
|
|
XR_934022.2:n.1802T>G
|
|
|
XR_934023.2:n.1823T>G
|
|
|
NM_000018.4:c.1841T>G
MANE Select
|
NP_000009.1:p.Ile614Ser
|
|
NM_001033859.3:c.1775T>G
|
NP_001029031.1:p.Ile592Ser
|
|
NM_001270447.2:c.1910T>G
|
NP_001257376.1:p.Ile637Ser
|
|
NM_001270448.2:c.1613T>G
|
NP_001257377.1:p.Ile538Ser
|
|