ENST00000298139.7:c.3425A>G
MANE Select
|
ENSP00000298139.5:p.Gln1142Arg
|
|
ENST00000650667.1:c.*3039A>G
|
ENSP00000498593.1:n.*3039A>G
|
|
ENST00000298139.5:c.3425A>G
|
ENSP00000298139.5:p.Gln1142Arg
|
|
ENST00000521620.5:n.2058A>G
|
|
|
NM_000553.4:c.3425A>G , LRG_524t1:c.3425A>G
|
NP_000544.2:p.Gln1142Arg
|
|
XM_011544639.1:c.3344A>G
|
XP_011542941.1:p.Gln1115Arg
|
|
XM_011544640.1:c.1826A>G
|
XP_011542942.1:p.Gln609Arg
|
|
XR_949470.1:n.3698A>G
|
|
|
XR_949471.1:n.3698A>G
|
|
|
XR_949472.1:n.3698A>G
|
|
|
XR_949643.1:n.614+1414T>C
|
|
|
NM_000553.5:c.3425A>G
|
NP_000544.2:p.Gln1142Arg
|
|
XM_011544639.3:c.3344A>G
|
XP_011542941.1:p.Gln1115Arg
|
|
XM_024447265.1:c.3215A>G
|
XP_024303033.1:p.Gln1072Arg
|
|
XR_949470.3:n.3726A>G
|
|
|
XR_949471.3:n.3726A>G
|
|
|
XR_949472.3:n.3726A>G
|
|
|
NM_000553.6:c.3425A>G
MANE Select
|
NP_000544.2:p.Gln1142Arg
|
|