ENST00000312465.12:c.616G>T
MANE Select
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ENSP00000311697.7:p.Val206Phe
|
|
ENST00000312465.11:c.616G>T
|
ENSP00000311697.7:p.Val206Phe
|
|
ENST00000456523.3:c.*140G>T
|
ENSP00000398353.3:n.*140G>T
|
|
ENST00000503413.1:n.565G>T
|
|
|
ENST00000507780.1:c.342+11469G>T
|
ENSP00000423903.1:n.342+11469G>T
|
|
NM_001291812.1:c.187G>T
|
NP_001278741.1:p.Val63Phe
|
|
NM_004464.3:c.616G>T
|
NP_004455.2:p.Val206Phe
|
|
NM_033143.2:c.*140G>T
|
NP_149134.1:n.*140G>T
|
|
NM_001291812.2:c.187G>T
|
NP_001278741.1:p.Val63Phe
|
|
NM_004464.4:c.616G>T
MANE Select
|
NP_004455.2:p.Val206Phe
|
|