ENST00000298139.7:c.3221T>G
MANE Select
|
ENSP00000298139.5:p.Leu1074Trp
|
|
ENST00000650667.1:c.*2835T>G
|
ENSP00000498593.1:n.*2835T>G
|
|
ENST00000298139.5:c.3221T>G
|
ENSP00000298139.5:p.Leu1074Trp
|
|
ENST00000521620.5:n.1854T>G
|
|
|
NM_000553.4:c.3221T>G , LRG_524t1:c.3221T>G
|
NP_000544.2:p.Leu1074Trp
|
|
XM_011544639.1:c.3140T>G
|
XP_011542941.1:p.Leu1047Trp
|
|
XM_011544640.1:c.1622T>G
|
XP_011542942.1:p.Leu541Trp
|
|
XR_949470.1:n.3494T>G
|
|
|
XR_949471.1:n.3494T>G
|
|
|
XR_949472.1:n.3494T>G
|
|
|
NM_000553.5:c.3221T>G
|
NP_000544.2:p.Leu1074Trp
|
|
XM_011544639.3:c.3140T>G
|
XP_011542941.1:p.Leu1047Trp
|
|
XM_024447265.1:c.3011T>G
|
XP_024303033.1:p.Leu1004Trp
|
|
XR_949470.3:n.3522T>G
|
|
|
XR_949471.3:n.3522T>G
|
|
|
XR_949472.3:n.3522T>G
|
|
|
NM_000553.6:c.3221T>G
MANE Select
|
NP_000544.2:p.Leu1074Trp
|
|