ENST00000272371.7:c.5827A>C
MANE Select
|
ENSP00000272371.2:p.Ser1943Arg
|
|
ENST00000339598.8:c.3512+455A>C
MANE Plus Clinical
|
ENSP00000344521.3:n.3512+455A>C
|
|
ENST00000402415.8:c.3586A>C
|
ENSP00000383906.4:p.Ser1196Arg
|
|
ENST00000272371.6:c.5827A>C
|
ENSP00000272371.2:p.Ser1943Arg
|
|
ENST00000338581.10:c.3526A>C
|
ENSP00000345137.6:p.Ser1176Arg
|
|
ENST00000339598.7:c.3512+455A>C
|
ENSP00000344521.3:n.3512+455A>C
|
|
ENST00000402415.7:c.3757A>C
|
ENSP00000383906.3:p.Ser1253Arg
|
|
ENST00000403946.7:c.5813+455A>C
|
ENSP00000385255.3:n.5813+455A>C
|
|
NM_001287489.1:c.5813+455A>C
|
NP_001274418.1:n.5813+455A>C
|
|
NM_004802.3:c.3526A>C
|
NP_004793.2:p.Ser1176Arg
|
|
NM_194248.2:c.5827A>C
|
NP_919224.1:p.Ser1943Arg
|
|
NM_194322.2:c.3757A>C
|
NP_919303.1:p.Ser1253Arg
|
|
NM_194323.2:c.3512+455A>C
|
NP_919304.1:n.3512+455A>C
|
|
XM_005264644.2:c.5798+455A>C
|
XP_005264701.1:n.5798+455A>C
|
|
XM_011533185.1:c.5858+455A>C
|
XP_011531487.1:n.5858+455A>C
|
|
XM_017005338.1:c.5767A>C
|
XP_016860827.1:p.Ser1923Arg
|
|
NM_001287489.2:c.5813+455A>C
|
NP_001274418.1:n.5813+455A>C
|
|
NM_004802.4:c.3526A>C
|
NP_004793.2:p.Ser1176Arg
|
|
NM_194248.3:c.5827A>C
MANE Select
|
NP_919224.1:p.Ser1943Arg
|
|
NM_194322.3:c.3757A>C
|
NP_919303.1:p.Ser1253Arg
|
|
NM_194323.3:c.3512+455A>C
MANE Plus Clinical
|
NP_919304.1:n.3512+455A>C
|
|