ENST00000262493.12:c.787A>T
MANE Select
|
ENSP00000262493.6:p.Thr263Ser
|
|
ENST00000562316.6:c.454A>T
|
ENSP00000457238.2:p.Thr152Ser
|
|
ENST00000564727.2:c.91A>T
|
ENSP00000454971.2:p.Thr31Ser
|
|
ENST00000568375.2:c.116-3419A>T
|
|
|
ENST00000638185.1:n.1002A>T
|
|
|
ENST00000638210.1:n.1087A>T
|
|
|
ENST00000638705.1:c.787A>T
|
ENSP00000491223.1:p.Thr263Ser
|
|
ENST00000638836.1:n.697A>T
|
|
|
ENST00000639055.1:n.1508A>T
|
|
|
ENST00000639251.1:n.688A>T
|
|
|
ENST00000639268.1:c.422A>T
|
|
|
ENST00000639341.1:c.312A>T
|
|
|
ENST00000639770.1:c.825A>T
|
ENSP00000491999.1:n.825A>T
|
|
ENST00000640390.1:n.717A>T
|
|
|
ENST00000640469.1:c.151A>T
|
ENSP00000491875.1:p.Thr51Ser
|
|
ENST00000640560.1:n.563A>T
|
|
|
ENST00000640893.1:c.*185A>T
|
ENSP00000492677.1:n.*185A>T
|
|
ENST00000262493.10:c.787A>T
|
ENSP00000262493.6:p.Thr263Ser
|
|
ENST00000564727.1:c.7A>T
|
ENSP00000454971.1:p.Thr3Ser
|
|
ENST00000568375.1:n.116-3419A>T
|
|
|
NM_020988.2:c.787A>T
|
NP_066268.1:p.Thr263Ser
|
|
XM_011523003.1:c.661A>T
|
XP_011521305.1:p.Thr221Ser
|
|
XM_011523003.3:c.661A>T
|
XP_011521305.1:p.Thr221Ser
|
|
NM_020988.3:c.787A>T
MANE Select
|
NP_066268.1:p.Thr263Ser
|
|