ENST00000272371.7:c.4796C>A
MANE Select
|
ENSP00000272371.2:p.Ser1599Tyr
|
|
ENST00000339598.8:c.2495C>A
MANE Plus Clinical
|
ENSP00000344521.3:p.Ser832Tyr
|
|
ENST00000402415.8:c.2555C>A
|
ENSP00000383906.4:p.Ser852Tyr
|
|
ENST00000272371.6:c.4796C>A
|
ENSP00000272371.2:p.Ser1599Tyr
|
|
ENST00000338581.10:c.2495C>A
|
ENSP00000345137.6:p.Ser832Tyr
|
|
ENST00000339598.7:c.2495C>A
|
ENSP00000344521.3:p.Ser832Tyr
|
|
ENST00000402415.7:c.2726C>A
|
ENSP00000383906.3:p.Ser909Tyr
|
|
ENST00000403946.7:c.4796C>A
|
ENSP00000385255.3:p.Ser1599Tyr
|
|
ENST00000464574.1:n.545C>A
|
|
|
NM_001287489.1:c.4796C>A
|
NP_001274418.1:p.Ser1599Tyr
|
|
NM_004802.3:c.2495C>A
|
NP_004793.2:p.Ser832Tyr
|
|
NM_194248.2:c.4796C>A
|
NP_919224.1:p.Ser1599Tyr
|
|
NM_194322.2:c.2726C>A
|
NP_919303.1:p.Ser909Tyr
|
|
NM_194323.2:c.2495C>A
|
NP_919304.1:p.Ser832Tyr
|
|
XM_005264644.2:c.4781C>A
|
XP_005264701.1:p.Ser1594Tyr
|
|
XM_011533185.1:c.4841C>A
|
XP_011531487.1:p.Ser1614Tyr
|
|
XM_017005338.1:c.4736C>A
|
XP_016860827.1:p.Ser1579Tyr
|
|
NM_001287489.2:c.4796C>A
|
NP_001274418.1:p.Ser1599Tyr
|
|
NM_004802.4:c.2495C>A
|
NP_004793.2:p.Ser832Tyr
|
|
NM_194248.3:c.4796C>A
MANE Select
|
NP_919224.1:p.Ser1599Tyr
|
|
NM_194322.3:c.2726C>A
|
NP_919303.1:p.Ser909Tyr
|
|
NM_194323.3:c.2495C>A
MANE Plus Clinical
|
NP_919304.1:p.Ser832Tyr
|
|