|
ENST00000356839.10:c.1628T>G
MANE Select
|
ENSP00000349297.5:p.Phe543Cys
|
|
|
ENST00000322910.9:c.*1583T>G
|
ENSP00000325395.5:n.*1583T>G
|
|
|
ENST00000350303.9:c.1562T>G
|
ENSP00000344152.5:p.Phe521Cys
|
|
|
ENST00000356839.9:c.1628T>G
|
ENSP00000349297.5:p.Phe543Cys
|
|
|
ENST00000542255.6:c.486T>G
|
|
|
|
ENST00000543245.6:c.1697T>G
|
ENSP00000438689.2:p.Phe566Cys
|
|
|
ENST00000578319.5:n.209T>G
|
|
|
|
ENST00000578711.1:n.998T>G
|
|
|
|
ENST00000578809.5:n.200T>G
|
|
|
|
ENST00000579391.1:n.232T>G
|
|
|
|
ENST00000579425.5:n.744T>G
|
|
|
|
ENST00000579546.1:c.363T>G
|
|
|
|
ENST00000579894.5:n.415T>G
|
|
|
|
ENST00000582450.1:n.136T>G
|
|
|
|
ENST00000583074.5:n.249T>G
|
|
|
|
ENST00000583848.5:c.14T>G
|
ENSP00000466487.1:p.Phe5Cys
|
|
|
ENST00000583850.5:n.399T>G
|
|
|
|
ENST00000583858.5:c.559T>G
|
|
|
|
ENST00000585203.6:n.819T>G
|
|
|
|
NM_000018.3:c.1628T>G
|
NP_000009.1:p.Phe543Cys
|
|
|
NM_001033859.2:c.1562T>G
|
NP_001029031.1:p.Phe521Cys
|
|
|
NM_001270447.1:c.1697T>G
|
NP_001257376.1:p.Phe566Cys
|
|
|
NM_001270448.1:c.1400T>G
|
NP_001257377.1:p.Phe467Cys
|
|
|
XM_006721516.2:c.1628T>G
|
XP_006721579.2:p.Phe543Cys
|
|
|
XM_011523829.1:c.1526T>G
|
XP_011522131.1:p.Phe509Cys
|
|
|
XM_011523830.1:c.1526T>G
|
XP_011522132.1:p.Phe509Cys
|
|
|
XR_934021.1:n.1731T>G
|
|
|
|
XR_934022.1:n.1637T>G
|
|
|
|
XR_934023.1:n.1637T>G
|
|
|
|
XM_006721516.3:c.1628T>G
|
XP_006721579.2:p.Phe543Cys
|
|
|
XM_011523829.2:c.1526T>G
|
XP_011522131.1:p.Phe509Cys
|
|
|
XM_011523830.2:c.1526T>G
|
XP_011522132.1:p.Phe509Cys
|
|
|
XM_024450741.1:c.1616T>G
|
XP_024306509.1:p.Phe539Cys
|
|
|
XR_934021.2:n.1683T>G
|
|
|
|
XR_934022.2:n.1589T>G
|
|
|
|
XR_934023.2:n.1589T>G
|
|
|
|
NM_000018.4:c.1628T>G
MANE Select
|
NP_000009.1:p.Phe543Cys
|
|
|
NM_001033859.3:c.1562T>G
|
NP_001029031.1:p.Phe521Cys
|
|
|
NM_001270447.2:c.1697T>G
|
NP_001257376.1:p.Phe566Cys
|
|
|
NM_001270448.2:c.1400T>G
|
NP_001257377.1:p.Phe467Cys
|
|
