ENST00000298139.7:c.3430G>T
MANE Select
|
ENSP00000298139.5:p.Val1144Phe
|
|
ENST00000650667.1:c.*3044G>T
|
ENSP00000498593.1:n.*3044G>T
|
|
ENST00000298139.5:c.3430G>T
|
ENSP00000298139.5:p.Val1144Phe
|
|
ENST00000521620.5:n.2063G>T
|
|
|
NM_000553.4:c.3430G>T , LRG_524t1:c.3430G>T
|
NP_000544.2:p.Val1144Phe
|
|
XM_011544639.1:c.3349G>T
|
XP_011542941.1:p.Val1117Phe
|
|
XM_011544640.1:c.1831G>T
|
XP_011542942.1:p.Val611Phe
|
|
XR_949470.1:n.3703G>T
|
|
|
XR_949471.1:n.3703G>T
|
|
|
XR_949472.1:n.3703G>T
|
|
|
XR_949643.1:n.614+1409C>A
|
|
|
NM_000553.5:c.3430G>T
|
NP_000544.2:p.Val1144Phe
|
|
XM_011544639.3:c.3349G>T
|
XP_011542941.1:p.Val1117Phe
|
|
XM_024447265.1:c.3220G>T
|
XP_024303033.1:p.Val1074Phe
|
|
XR_949470.3:n.3731G>T
|
|
|
XR_949471.3:n.3731G>T
|
|
|
XR_949472.3:n.3731G>T
|
|
|
NM_000553.6:c.3430G>T
MANE Select
|
NP_000544.2:p.Val1144Phe
|
|