ENST00000298139.7:c.3494A>T
MANE Select
|
ENSP00000298139.5:p.Gln1165Leu
|
|
ENST00000650667.1:c.*3108A>T
|
ENSP00000498593.1:n.*3108A>T
|
|
ENST00000298139.5:c.3494A>T
|
ENSP00000298139.5:p.Gln1165Leu
|
|
ENST00000521620.5:n.2127A>T
|
|
|
NM_000553.4:c.3494A>T , LRG_524t1:c.3494A>T
|
NP_000544.2:p.Gln1165Leu
|
|
XM_011544639.1:c.3413A>T
|
XP_011542941.1:p.Gln1138Leu
|
|
XM_011544640.1:c.1895A>T
|
XP_011542942.1:p.Gln632Leu
|
|
XR_949470.1:n.3767A>T
|
|
|
XR_949471.1:n.3767A>T
|
|
|
XR_949472.1:n.3767A>T
|
|
|
XR_949643.1:n.614+1110T>A
|
|
|
NM_000553.5:c.3494A>T
|
NP_000544.2:p.Gln1165Leu
|
|
XM_011544639.3:c.3413A>T
|
XP_011542941.1:p.Gln1138Leu
|
|
XM_024447265.1:c.3284A>T
|
XP_024303033.1:p.Gln1095Leu
|
|
XR_949470.3:n.3795A>T
|
|
|
XR_949471.3:n.3795A>T
|
|
|
XR_949472.3:n.3795A>T
|
|
|
NM_000553.6:c.3494A>T
MANE Select
|
NP_000544.2:p.Gln1165Leu
|
|