|
ENST00000641284.2:c.2382-7173A>G
|
ENSP00000493088.1:n.2382-7173A>G
|
|
|
ENST00000646677.2:c.*422A>G
|
ENSP00000496533.1:n.*422A>G
|
|
|
ENST00000697425.1:c.484A>G
|
|
|
|
ENST00000697426.1:c.372A>G
|
|
|
|
ENST00000697427.1:c.288A>G
|
|
|
|
ENST00000697428.1:n.2135A>G
|
|
|
|
ENST00000641284.1:c.2382-7173A>G
|
ENSP00000493088.1:n.2382-7173A>G
|
|
|
ENST00000646677.1:c.*422A>G
|
ENSP00000496533.1:n.*422A>G
|
|
|
ENST00000647318.2:c.2657A>G
MANE Select
|
ENSP00000495993.1:p.Asp886Gly
|
|
|
ENST00000300589.6:c.2738A>G
|
ENSP00000300589.2:p.Asp913Gly
|
|
|
ENST00000524712.5:c.232A>G
|
|
|
|
ENST00000527052.5:c.204A>G
|
|
|
|
ENST00000529633.5:c.316A>G
|
|
|
|
ENST00000534057.1:c.372A>G
|
|
|
|
ENST00000534067.5:c.468A>G
|
|
|
|
NM_001293557.1:c.2657A>G
|
NP_001280486.1:p.Asp886Gly
|
|
|
NM_022162.2:c.2738A>G
|
NP_071445.1:p.Asp913Gly
|
|
|
XM_005256084.2:c.2657A>G
|
XP_005256141.1:p.Asp886Gly
|
|
|
XM_006721242.2:c.2573A>G
|
XP_006721305.1:p.Asp858Gly
|
|
|
XM_011523257.1:c.2234A>G
|
XP_011521559.1:p.Asp745Gly
|
|
|
XM_011523258.1:c.2234A>G
|
XP_011521560.1:p.Asp745Gly
|
|
|
XM_011523259.1:c.2072A>G
|
XP_011521561.1:p.Asp691Gly
|
|
|
XR_429725.2:n.2579A>G
|
|
|
|
XR_429726.2:n.2495A>G
|
|
|
|
XR_933387.1:n.2775A>G
|
|
|
|
XM_005256084.4:c.2657A>G
|
XP_005256141.1:p.Asp886Gly
|
|
|
XM_006721242.4:c.2573A>G
|
XP_006721305.1:p.Asp858Gly
|
|
|
XM_011523259.2:c.2072A>G
|
XP_011521561.1:p.Asp691Gly
|
|
|
XM_017023535.1:c.2165A>G
|
XP_016879024.1:p.Asp722Gly
|
|
|
XM_017023536.1:c.2072A>G
|
XP_016879025.1:p.Asp691Gly
|
|
|
XM_017023537.1:c.2072A>G
|
XP_016879026.1:p.Asp691Gly
|
|
|
XM_017023538.1:c.2072A>G
|
XP_016879027.1:p.Asp691Gly
|
|
|
XR_429725.3:n.2532A>G
|
|
|
|
XR_429726.3:n.2448A>G
|
|
|
|
XR_933387.2:n.2728A>G
|
|
|
|
NM_001293557.2:c.2657A>G
|
NP_001280486.1:p.Asp886Gly
|
|
|
NM_001370466.1:c.2657A>G
MANE Select
|
NP_001357395.1:p.Asp886Gly
|
|
|
NM_022162.3:c.2738A>G
|
NP_071445.1:p.Asp913Gly
|
|
|
NR_163434.1:n.2869A>G
|
|
|
