|
ENST00000641284.2:c.2382-7129A>G
|
ENSP00000493088.1:n.2382-7129A>G
|
|
|
ENST00000646677.2:c.*466A>G
|
ENSP00000496533.1:n.*466A>G
|
|
|
ENST00000697425.1:c.528A>G
|
|
|
|
ENST00000697426.1:c.416A>G
|
|
|
|
ENST00000697427.1:c.332A>G
|
|
|
|
ENST00000697428.1:n.2179A>G
|
|
|
|
ENST00000641284.1:c.2382-7129A>G
|
ENSP00000493088.1:n.2382-7129A>G
|
|
|
ENST00000646677.1:c.*466A>G
|
ENSP00000496533.1:n.*466A>G
|
|
|
ENST00000647318.2:c.2701A>G
MANE Select
|
ENSP00000495993.1:p.Ser901Gly
|
|
|
ENST00000300589.6:c.2782A>G
|
ENSP00000300589.2:p.Ser928Gly
|
|
|
ENST00000524712.5:c.276A>G
|
|
|
|
ENST00000527052.5:c.248A>G
|
|
|
|
ENST00000529633.5:c.360A>G
|
|
|
|
ENST00000534057.1:c.416A>G
|
|
|
|
ENST00000534067.5:c.512A>G
|
|
|
|
NM_001293557.1:c.2701A>G
|
NP_001280486.1:p.Ser901Gly
|
|
|
NM_022162.2:c.2782A>G
|
NP_071445.1:p.Ser928Gly
|
|
|
XM_005256084.2:c.2701A>G
|
XP_005256141.1:p.Ser901Gly
|
|
|
XM_006721242.2:c.2617A>G
|
XP_006721305.1:p.Ser873Gly
|
|
|
XM_011523257.1:c.2278A>G
|
XP_011521559.1:p.Ser760Gly
|
|
|
XM_011523258.1:c.2278A>G
|
XP_011521560.1:p.Ser760Gly
|
|
|
XM_011523259.1:c.2116A>G
|
XP_011521561.1:p.Ser706Gly
|
|
|
XR_429725.2:n.2623A>G
|
|
|
|
XR_429726.2:n.2539A>G
|
|
|
|
XR_933387.1:n.2819A>G
|
|
|
|
XM_005256084.4:c.2701A>G
|
XP_005256141.1:p.Ser901Gly
|
|
|
XM_006721242.4:c.2617A>G
|
XP_006721305.1:p.Ser873Gly
|
|
|
XM_011523259.2:c.2116A>G
|
XP_011521561.1:p.Ser706Gly
|
|
|
XM_017023535.1:c.2209A>G
|
XP_016879024.1:p.Ser737Gly
|
|
|
XM_017023536.1:c.2116A>G
|
XP_016879025.1:p.Ser706Gly
|
|
|
XM_017023537.1:c.2116A>G
|
XP_016879026.1:p.Ser706Gly
|
|
|
XM_017023538.1:c.2116A>G
|
XP_016879027.1:p.Ser706Gly
|
|
|
XR_429725.3:n.2576A>G
|
|
|
|
XR_429726.3:n.2492A>G
|
|
|
|
XR_933387.2:n.2772A>G
|
|
|
|
NM_001293557.2:c.2701A>G
|
NP_001280486.1:p.Ser901Gly
|
|
|
NM_001370466.1:c.2701A>G
MANE Select
|
NP_001357395.1:p.Ser901Gly
|
|
|
NM_022162.3:c.2782A>G
|
NP_071445.1:p.Ser928Gly
|
|
|
NR_163434.1:n.2913A>G
|
|
|
