ENST00000262493.12:c.962G>T
MANE Select
|
ENSP00000262493.6:p.Cys321Phe
|
|
ENST00000562316.6:c.545-1153G>T
|
ENSP00000457238.2:n.545-1153G>T
|
|
ENST00000564727.2:c.266G>T
|
ENSP00000454971.2:p.Cys89Phe
|
|
ENST00000568375.2:c.200G>T
|
|
|
ENST00000638210.1:n.1262G>T
|
|
|
ENST00000638705.1:c.962G>T
|
ENSP00000491223.1:p.Cys321Phe
|
|
ENST00000638836.1:n.872G>T
|
|
|
ENST00000639251.1:n.863G>T
|
|
|
ENST00000639268.1:c.597G>T
|
|
|
ENST00000639341.1:c.487G>T
|
|
|
ENST00000639770.1:c.1000G>T
|
ENSP00000491999.1:n.1000G>T
|
|
ENST00000640390.1:n.892G>T
|
|
|
ENST00000640469.1:c.326G>T
|
ENSP00000491875.1:p.Cys109Phe
|
|
ENST00000640560.1:n.738G>T
|
|
|
ENST00000640893.1:c.*360G>T
|
ENSP00000492677.1:n.*360G>T
|
|
ENST00000262493.10:c.962G>T
|
ENSP00000262493.6:p.Cys321Phe
|
|
ENST00000564727.1:c.182G>T
|
ENSP00000454971.1:p.Cys61Phe
|
|
ENST00000568375.1:n.200G>T
|
|
|
NM_020988.2:c.962G>T
|
NP_066268.1:p.Cys321Phe
|
|
XM_011523003.1:c.836G>T
|
XP_011521305.1:p.Cys279Phe
|
|
XM_011523003.3:c.836G>T
|
XP_011521305.1:p.Cys279Phe
|
|
NM_020988.3:c.962G>T
MANE Select
|
NP_066268.1:p.Cys321Phe
|
|