ENST00000262493.12:c.864T=
MANE Select
|
ENSP00000262493.6:p.Phe288=
|
|
ENST00000562316.6:c.531T=
|
ENSP00000457238.2:p.Phe177=
|
|
ENST00000564727.2:c.168T=
|
ENSP00000454971.2:p.Phe56=
|
|
ENST00000568375.2:c.116-3342T=
|
|
|
ENST00000638185.1:n.1079T=
|
|
|
ENST00000638210.1:n.1164T=
|
|
|
ENST00000638705.1:c.864T=
|
ENSP00000491223.1:p.Phe288=
|
|
ENST00000638836.1:n.774T=
|
|
|
ENST00000639055.1:n.1585T=
|
|
|
ENST00000639251.1:n.765T=
|
|
|
ENST00000639268.1:c.499T=
|
|
|
ENST00000639341.1:c.389T=
|
|
|
ENST00000639770.1:c.902T=
|
ENSP00000491999.1:n.902T=
|
|
ENST00000640390.1:n.794T=
|
|
|
ENST00000640469.1:c.228T=
|
ENSP00000491875.1:p.Phe76=
|
|
ENST00000640560.1:n.640T=
|
|
|
ENST00000640893.1:c.*262T=
|
ENSP00000492677.1:n.*262T=
|
|
ENST00000262493.10:c.864T=
|
ENSP00000262493.6:p.Phe288=
|
|
ENST00000564727.1:c.84T=
|
ENSP00000454971.1:p.Phe28=
|
|
ENST00000568375.1:n.116-3342T=
|
|
|
NM_020988.2:c.864T=
|
NP_066268.1:p.Phe288=
|
|
XM_011523003.1:c.738T=
|
XP_011521305.1:p.Phe246=
|
|
XM_011523003.3:c.738T=
|
XP_011521305.1:p.Phe246=
|
|
NM_020988.3:c.864T=
MANE Select
|
NP_066268.1:p.Phe288=
|
|