ENST00000225927.7:c.1453G>T
MANE Select
|
ENSP00000225927.1:p.Val485Phe
|
|
ENST00000225927.6:c.1453G>T
|
ENSP00000225927.1:p.Val485Phe
|
|
ENST00000591587.1:c.791G>T
|
ENSP00000467836.1:n.791G>T
|
|
ENST00000592454.1:c.492G>T
|
|
|
NM_000263.3:c.1453G>T
|
NP_000254.2:p.Val485Phe
|
|
XM_006721920.2:c.622G>T
|
XP_006721983.1:p.Val208Phe
|
|
XM_011524840.1:c.454G>T
|
XP_011523142.1:p.Val152Phe
|
|
XM_017024687.1:c.622G>T
|
XP_016880176.1:p.Val208Phe
|
|
XM_024450771.1:c.1510G>T
|
XP_024306539.1:p.Val504Phe
|
|
XM_024450772.1:c.454G>T
|
XP_024306540.1:p.Val152Phe
|
|
NM_000263.4:c.1453G>T
MANE Select
|
NP_000254.2:p.Val485Phe
|
|