ENST00000262418.12:c.1951C>T
MANE Select
|
ENSP00000262418.6:p.His651Tyr
|
|
ENST00000262418.10:c.1951C>T
|
ENSP00000262418.6:p.His651Tyr
|
|
ENST00000399246.3:c.853C>T
|
ENSP00000382190.3:p.His285Tyr
|
|
NM_000342.3:c.1951C>T
|
NP_000333.1:p.His651Tyr
|
|
XM_005257593.3:c.1756C>T
|
XP_005257650.1:p.His586Tyr
|
|
XM_011525129.1:c.1861C>T
|
XP_011523431.1:p.His621Tyr
|
|
XM_011525130.1:c.1951C>T
|
XP_011523432.1:p.His651Tyr
|
|
XM_011525131.1:c.1951C>T
|
XP_011523433.1:p.His651Tyr
|
|
XM_005257593.5:c.1756C>T
|
XP_005257650.1:p.His586Tyr
|
|
XM_011525129.2:c.1861C>T
|
XP_011523431.1:p.His621Tyr
|
|
NM_000342.4:c.1951C>T
MANE Select
|
NP_000333.1:p.His651Tyr
|
|