ENST00000262493.12:c.871T>C
MANE Select
|
ENSP00000262493.6:p.Tyr291His
|
|
ENST00000562316.6:c.538T>C
|
ENSP00000457238.2:p.Tyr180His
|
|
ENST00000564727.2:c.175T>C
|
ENSP00000454971.2:p.Tyr59His
|
|
ENST00000568375.2:c.116-3335T>C
|
|
|
ENST00000638185.1:n.1086T>C
|
|
|
ENST00000638210.1:n.1171T>C
|
|
|
ENST00000638705.1:c.871T>C
|
ENSP00000491223.1:p.Tyr291His
|
|
ENST00000638836.1:n.781T>C
|
|
|
ENST00000639055.1:n.1592T>C
|
|
|
ENST00000639251.1:n.772T>C
|
|
|
ENST00000639268.1:c.506T>C
|
|
|
ENST00000639341.1:c.396T>C
|
|
|
ENST00000639770.1:c.909T>C
|
ENSP00000491999.1:n.909T>C
|
|
ENST00000640390.1:n.801T>C
|
|
|
ENST00000640469.1:c.235T>C
|
ENSP00000491875.1:p.Tyr79His
|
|
ENST00000640560.1:n.647T>C
|
|
|
ENST00000640893.1:c.*269T>C
|
ENSP00000492677.1:n.*269T>C
|
|
ENST00000262493.10:c.871T>C
|
ENSP00000262493.6:p.Tyr291His
|
|
ENST00000564727.1:c.91T>C
|
ENSP00000454971.1:p.Tyr31His
|
|
ENST00000568375.1:n.116-3335T>C
|
|
|
NM_020988.2:c.871T>C
|
NP_066268.1:p.Tyr291His
|
|
XM_011523003.1:c.745T>C
|
XP_011521305.1:p.Tyr249His
|
|
XM_011523003.3:c.745T>C
|
XP_011521305.1:p.Tyr249His
|
|
NM_020988.3:c.871T>C
MANE Select
|
NP_066268.1:p.Tyr291His
|
|