ENST00000225927.7:c.2105T>A
MANE Select
|
ENSP00000225927.1:p.Phe702Tyr
|
|
ENST00000225927.6:c.2105T>A
|
ENSP00000225927.1:p.Phe702Tyr
|
|
ENST00000591587.1:c.1443T>A
|
ENSP00000467836.1:n.1443T>A
|
|
NM_000263.3:c.2105T>A
|
NP_000254.2:p.Phe702Tyr
|
|
XM_006721920.2:c.1274T>A
|
XP_006721983.1:p.Phe425Tyr
|
|
XM_011524840.1:c.1106T>A
|
XP_011523142.1:p.Phe369Tyr
|
|
XM_017024687.1:c.1274T>A
|
XP_016880176.1:p.Phe425Tyr
|
|
XM_024450771.1:c.2162T>A
|
XP_024306539.1:p.Phe721Tyr
|
|
XM_024450772.1:c.1106T>A
|
XP_024306540.1:p.Phe369Tyr
|
|
NM_000263.4:c.2105T>A
MANE Select
|
NP_000254.2:p.Phe702Tyr
|
|