ENST00000527168.6:n.541C>G
|
|
|
ENST00000529110.2:c.526C>G
|
ENSP00000435349.2:p.Leu176Val
|
|
ENST00000529957.6:n.500C>G
|
|
|
ENST00000683366.1:c.*174C>G
|
ENSP00000507283.1:n.*174C>G
|
|
ENST00000683887.1:c.490C>G
|
ENSP00000506886.1:p.Leu164Val
|
|
ENST00000684100.1:n.436C>G
|
|
|
ENST00000684126.1:n.500C>G
|
|
|
ENST00000684688.1:n.1067C>G
|
|
|
ENST00000204679.9:c.442C>G
MANE Select
|
ENSP00000204679.4:p.Leu148Val
|
|
ENST00000204679.8:c.442C>G
|
ENSP00000204679.4:p.Leu148Val
|
|
ENST00000527076.1:n.1458C>G
|
|
|
ENST00000527168.5:n.478C>G
|
|
|
ENST00000529110.1:c.509C>G
|
|
|
ENST00000529957.5:n.541C>G
|
|
|
NM_032520.4:c.442C>G
|
NP_115909.1:p.Leu148Val
|
|
XM_017023782.1:c.490C>G
|
XP_016879271.1:p.Leu164Val
|
|
XM_017023783.1:c.82C>G
|
XP_016879272.1:p.Leu28Val
|
|
NM_032520.5:c.442C>G
MANE Select
|
NP_115909.1:p.Leu148Val
|
|