ENST00000403665.7:c.1452G=
MANE Select
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ENSP00000384957.2:p.Leu484=
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|
ENST00000264691.4:c.148G=
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|
|
ENST00000264692.8:c.1290G=
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ENSP00000264692.5:p.Leu430=
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|
ENST00000403665.6:c.1452G=
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ENSP00000384957.2:p.Leu484=
|
|
NM_000128.3:c.1452G= , LRG_583t1:c.1452G=
|
NP_000119.1:p.Leu484=
|
|
XM_005262821.2:c.1455G=
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XP_005262878.1:p.Leu485=
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|
XM_005262822.2:c.1455G=
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XP_005262879.1:p.Leu485=
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|
XM_005262823.2:c.1185G=
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XP_005262880.1:p.Leu395=
|
|
XM_005262824.1:c.1455G=
|
XP_005262881.1:p.Leu485=
|
|
XM_006714137.1:c.1407G=
|
XP_006714200.1:p.Leu469=
|
|
XR_938706.1:n.1860G=
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|
|
XR_938707.1:n.1860G=
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|
|
XM_005262821.4:c.1455G=
|
XP_005262878.1:p.Leu485=
|
|
XM_005262822.4:c.1455G=
|
XP_005262879.1:p.Leu485=
|
|
XM_005262823.4:c.1185G=
|
XP_005262880.1:p.Leu395=
|
|
XM_006714137.3:c.1407G=
|
XP_006714200.1:p.Leu469=
|
|
XR_001741172.2:n.1926G=
|
|
|
NM_000128.4:c.1452G=
MANE Select
|
NP_000119.1:p.Leu484=
|
|