ENST00000264381.8:c.1102G>T
MANE Select
|
ENSP00000264381.3:p.Asp368Tyr
|
|
ENST00000264381.7:c.1102G>T
|
ENSP00000264381.3:p.Asp368Tyr
|
|
ENST00000479451.5:c.107+7382G>T
|
ENSP00000418325.1:n.107+7382G>T
|
|
ENST00000482958.1:c.1102G>T
|
ENSP00000419804.1:p.Asp368Tyr
|
|
ENST00000488954.1:c.107+7382G>T
|
ENSP00000418504.1:n.107+7382G>T
|
|
ENST00000497011.5:c.1102G>T
|
ENSP00000419505.1:p.Asp368Tyr
|
|
NM_000055.2:c.1102G>T
|
NP_000046.1:p.Asp368Tyr
|
|
XM_005247685.1:c.1225G>T
|
XP_005247742.1:p.Asp409Tyr
|
|
NM_000055.3:c.1102G>T
|
NP_000046.1:p.Asp368Tyr
|
|
NR_137635.1:n.159+7382G>T
|
|
|
NR_137636.1:n.1269G>T
|
|
|
NM_000055.4:c.1102G>T
MANE Select
|
NP_000046.1:p.Asp368Tyr
|
|
NR_137635.2:n.110+7382G>T
|
|
|
NR_137636.2:n.1220G>T
|
|
|