ENST00000356839.10:c.1868C>T
MANE Select
|
ENSP00000349297.5:p.Ser623Phe
|
|
ENST00000322910.9:c.*1823C>T
|
ENSP00000325395.5:n.*1823C>T
|
|
ENST00000350303.9:c.1802C>T
|
ENSP00000344152.5:p.Ser601Phe
|
|
ENST00000356839.9:c.1868C>T
|
ENSP00000349297.5:p.Ser623Phe
|
|
ENST00000542255.6:c.747C>T
|
|
|
ENST00000543245.6:c.1937C>T
|
ENSP00000438689.2:p.Ser646Phe
|
|
ENST00000578033.1:n.293C>T
|
|
|
ENST00000578319.5:n.449C>T
|
|
|
ENST00000578711.1:n.1493C>T
|
|
|
ENST00000578809.5:n.440C>T
|
|
|
ENST00000579425.5:n.984C>T
|
|
|
ENST00000583848.5:c.234C>T
|
ENSP00000466487.1:n.234C>T
|
|
ENST00000583850.5:n.639C>T
|
|
|
ENST00000583858.5:c.799C>T
|
|
|
NM_000018.3:c.1868C>T
|
NP_000009.1:p.Ser623Phe
|
|
NM_001033859.2:c.1802C>T
|
NP_001029031.1:p.Ser601Phe
|
|
NM_001270447.1:c.1937C>T
|
NP_001257376.1:p.Ser646Phe
|
|
NM_001270448.1:c.1640C>T
|
NP_001257377.1:p.Ser547Phe
|
|
XM_006721516.2:c.1889C>T
|
XP_006721579.2:p.Ser630Phe
|
|
XM_011523829.1:c.1787C>T
|
XP_011522131.1:p.Ser596Phe
|
|
XM_011523830.1:c.1766C>T
|
XP_011522132.1:p.Ser589Phe
|
|
XR_934021.1:n.1971C>T
|
|
|
XR_934022.1:n.1877C>T
|
|
|
XR_934023.1:n.1898C>T
|
|
|
XM_006721516.3:c.1889C>T
|
XP_006721579.2:p.Ser630Phe
|
|
XM_011523829.2:c.1787C>T
|
XP_011522131.1:p.Ser596Phe
|
|
XM_011523830.2:c.1766C>T
|
XP_011522132.1:p.Ser589Phe
|
|
XM_024450741.1:c.1856C>T
|
XP_024306509.1:p.Ser619Phe
|
|
XR_934021.2:n.1923C>T
|
|
|
XR_934022.2:n.1829C>T
|
|
|
XR_934023.2:n.1850C>T
|
|
|
NM_000018.4:c.1868C>T
MANE Select
|
NP_000009.1:p.Ser623Phe
|
|
NM_001033859.3:c.1802C>T
|
NP_001029031.1:p.Ser601Phe
|
|
NM_001270447.2:c.1937C>T
|
NP_001257376.1:p.Ser646Phe
|
|
NM_001270448.2:c.1640C>T
|
NP_001257377.1:p.Ser547Phe
|
|