ENST00000262494.13:c.596T>A
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ENSP00000262494.7:p.Leu199Gln
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|
ENST00000262493.12:c.596T>A
MANE Select
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ENSP00000262493.6:p.Leu199Gln
|
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ENST00000262494.12:c.596T>A
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ENSP00000262494.7:p.Leu199Gln
|
|
ENST00000562316.6:c.263T>A
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ENSP00000457238.2:p.Leu88Gln
|
|
ENST00000638185.1:n.811T>A
|
|
|
ENST00000638210.1:n.896T>A
|
|
|
ENST00000638705.1:c.596T>A
|
ENSP00000491223.1:p.Leu199Gln
|
|
ENST00000638836.1:n.506T>A
|
|
|
ENST00000639055.1:n.1317T>A
|
|
|
ENST00000639251.1:n.497T>A
|
|
|
ENST00000639268.1:c.231T>A
|
|
|
ENST00000639341.1:c.121T>A
|
|
|
ENST00000639770.1:c.634T>A
|
ENSP00000491999.1:n.634T>A
|
|
ENST00000640390.1:n.526T>A
|
|
|
ENST00000640560.1:n.372T>A
|
|
|
ENST00000640893.1:c.435T>A
|
ENSP00000492677.1:p.Ala145=
|
|
ENST00000262493.10:c.596T>A
|
ENSP00000262493.6:p.Leu199Gln
|
|
ENST00000262494.11:c.596T>A
|
ENSP00000262494.7:p.Leu199Gln
|
|
NM_020988.2:c.596T>A
|
NP_066268.1:p.Leu199Gln
|
|
NM_138736.2:c.596T>A
|
NP_620073.2:p.Leu199Gln
|
|
XM_011523003.1:c.470T>A
|
XP_011521305.1:p.Leu157Gln
|
|
XM_011523003.3:c.470T>A
|
XP_011521305.1:p.Leu157Gln
|
|
NM_020988.3:c.596T>A
MANE Select
|
NP_066268.1:p.Leu199Gln
|
|
NM_138736.3:c.596T>A
|
NP_620073.2:p.Leu199Gln
|
|