ENST00000338639.10:c.453G=
MANE Select
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ENSP00000340278.5:p.Leu151=
|
|
ENST00000338639.9:c.453G=
|
ENSP00000340278.5:p.Leu151=
|
|
ENST00000377488.5:c.453G=
|
ENSP00000366708.1:p.Leu151=
|
|
ENST00000377491.5:c.453G=
|
ENSP00000366711.1:p.Leu151=
|
|
ENST00000377493.9:c.393G=
|
ENSP00000466242.1:p.Leu131=
|
|
ENST00000469225.1:c.366G=
|
ENSP00000466756.1:p.Leu122=
|
|
ENST00000493373.5:c.453G=
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ENSP00000465404.1:p.Leu151=
|
|
ENST00000493678.5:c.453G=
|
ENSP00000418770.1:p.Leu151=
|
|
NM_001123377.1:c.453G=
|
NP_001116849.1:p.Leu151=
|
|
NM_007262.4:c.453G=
|
NP_009193.2:p.Leu151=
|
|
XM_005263424.2:c.453G=
|
XP_005263481.1:p.Leu151=
|
|
XM_005263424.3:c.453G=
|
XP_005263481.1:p.Leu151=
|
|
NM_007262.5:c.453G=
MANE Select
|
NP_009193.2:p.Leu151=
|
|
NM_001123377.2:c.453G=
|
NP_001116849.1:p.Leu151=
|
|