ENST00000409709.9:c.6617G>T
MANE Select
|
ENSP00000386331.3:p.Ser2206Ile
|
|
ENST00000670577.1:c.4418G>T
|
|
|
ENST00000409619.6:c.6470G>T
|
ENSP00000386635.2:p.Ser2157Ile
|
|
ENST00000409709.7:c.6617G>T
|
ENSP00000386331.3:p.Ser2206Ile
|
|
ENST00000458169.2:c.4043G>T
|
ENSP00000417017.2:p.Ser1348Ile
|
|
ENST00000458637.6:c.6497G>T
|
ENSP00000392185.2:p.Ser2166Ile
|
|
ENST00000481328.7:n.5167G>T
|
|
|
ENST00000605744.1:n.2131G>T
|
|
|
NM_000260.3:c.6617G>T
|
NP_000251.3:p.Ser2206Ile
|
|
NM_001127180.1:c.6497G>T
|
NP_001120652.1:p.Ser2166Ile
|
|
XM_005274012.2:c.6500G>T
|
XP_005274069.1:p.Ser2167Ile
|
|
XM_006718561.2:c.6503G>T
|
XP_006718624.1:p.Ser2168Ile
|
|
XR_949941.1:n.6911G>T
|
|
|
XM_017017780.1:c.6707G>T
|
XP_016873269.1:p.Ser2236Ile
|
|
XM_017017784.1:c.6590G>T
|
XP_016873273.1:p.Ser2197Ile
|
|
XM_017017788.1:c.6593G>T
|
XP_016873277.1:p.Ser2198Ile
|
|
XR_001747885.1:n.6696G>T
|
|
|
XR_001747887.1:n.6682G>T
|
|
|
NM_000260.4:c.6617G>T
MANE Select
|
NP_000251.3:p.Ser2206Ile
|
|
NM_001127180.2:c.6497G>T
|
NP_001120652.1:p.Ser2166Ile
|
|
NM_001369365.1:c.6470G>T
|
NP_001356294.1:p.Ser2157Ile
|
|