ENST00000356839.10:c.1868C>G
MANE Select
|
ENSP00000349297.5:p.Ser623Cys
|
|
ENST00000322910.9:c.*1823C>G
|
ENSP00000325395.5:n.*1823C>G
|
|
ENST00000350303.9:c.1802C>G
|
ENSP00000344152.5:p.Ser601Cys
|
|
ENST00000356839.9:c.1868C>G
|
ENSP00000349297.5:p.Ser623Cys
|
|
ENST00000542255.6:c.747C>G
|
|
|
ENST00000543245.6:c.1937C>G
|
ENSP00000438689.2:p.Ser646Cys
|
|
ENST00000578033.1:n.293C>G
|
|
|
ENST00000578319.5:n.449C>G
|
|
|
ENST00000578711.1:n.1493C>G
|
|
|
ENST00000578809.5:n.440C>G
|
|
|
ENST00000579425.5:n.984C>G
|
|
|
ENST00000583848.5:c.234C>G
|
ENSP00000466487.1:n.234C>G
|
|
ENST00000583850.5:n.639C>G
|
|
|
ENST00000583858.5:c.799C>G
|
|
|
NM_000018.3:c.1868C>G
|
NP_000009.1:p.Ser623Cys
|
|
NM_001033859.2:c.1802C>G
|
NP_001029031.1:p.Ser601Cys
|
|
NM_001270447.1:c.1937C>G
|
NP_001257376.1:p.Ser646Cys
|
|
NM_001270448.1:c.1640C>G
|
NP_001257377.1:p.Ser547Cys
|
|
XM_006721516.2:c.1889C>G
|
XP_006721579.2:p.Ser630Cys
|
|
XM_011523829.1:c.1787C>G
|
XP_011522131.1:p.Ser596Cys
|
|
XM_011523830.1:c.1766C>G
|
XP_011522132.1:p.Ser589Cys
|
|
XR_934021.1:n.1971C>G
|
|
|
XR_934022.1:n.1877C>G
|
|
|
XR_934023.1:n.1898C>G
|
|
|
XM_006721516.3:c.1889C>G
|
XP_006721579.2:p.Ser630Cys
|
|
XM_011523829.2:c.1787C>G
|
XP_011522131.1:p.Ser596Cys
|
|
XM_011523830.2:c.1766C>G
|
XP_011522132.1:p.Ser589Cys
|
|
XM_024450741.1:c.1856C>G
|
XP_024306509.1:p.Ser619Cys
|
|
XR_934021.2:n.1923C>G
|
|
|
XR_934022.2:n.1829C>G
|
|
|
XR_934023.2:n.1850C>G
|
|
|
NM_000018.4:c.1868C>G
MANE Select
|
NP_000009.1:p.Ser623Cys
|
|
NM_001033859.3:c.1802C>G
|
NP_001029031.1:p.Ser601Cys
|
|
NM_001270447.2:c.1937C>G
|
NP_001257376.1:p.Ser646Cys
|
|
NM_001270448.2:c.1640C>G
|
NP_001257377.1:p.Ser547Cys
|
|