ENST00000262493.12:c.776T>A
MANE Select
|
ENSP00000262493.6:p.Phe259Tyr
|
|
ENST00000562316.6:c.443T>A
|
ENSP00000457238.2:p.Phe148Tyr
|
|
ENST00000564727.2:c.80T>A
|
ENSP00000454971.2:p.Phe27Tyr
|
|
ENST00000568375.2:c.116-3430T>A
|
|
|
ENST00000638185.1:n.991T>A
|
|
|
ENST00000638210.1:n.1076T>A
|
|
|
ENST00000638705.1:c.776T>A
|
ENSP00000491223.1:p.Phe259Tyr
|
|
ENST00000638836.1:n.686T>A
|
|
|
ENST00000639055.1:n.1497T>A
|
|
|
ENST00000639251.1:n.677T>A
|
|
|
ENST00000639268.1:c.411T>A
|
|
|
ENST00000639341.1:c.301T>A
|
|
|
ENST00000639770.1:c.814T>A
|
ENSP00000491999.1:n.814T>A
|
|
ENST00000640390.1:n.706T>A
|
|
|
ENST00000640469.1:c.140T>A
|
ENSP00000491875.1:p.Phe47Tyr
|
|
ENST00000640560.1:n.552T>A
|
|
|
ENST00000640893.1:c.*174T>A
|
ENSP00000492677.1:n.*174T>A
|
|
ENST00000262493.10:c.776T>A
|
ENSP00000262493.6:p.Phe259Tyr
|
|
ENST00000568375.1:n.116-3430T>A
|
|
|
NM_020988.2:c.776T>A
|
NP_066268.1:p.Phe259Tyr
|
|
XM_011523003.1:c.650T>A
|
XP_011521305.1:p.Phe217Tyr
|
|
XM_011523003.3:c.650T>A
|
XP_011521305.1:p.Phe217Tyr
|
|
NM_020988.3:c.776T>A
MANE Select
|
NP_066268.1:p.Phe259Tyr
|
|