ENST00000592092.2:n.735T=
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|
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ENST00000673918.2:c.6363T=
|
ENSP00000501283.1:p.Ala2121=
|
|
ENST00000674114.2:c.3970T=
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ENSP00000501039.2:n.3970T=
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ENST00000684977.1:c.1647T=
|
ENSP00000509384.1:p.Ala549=
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|
ENST00000689544.1:n.1582T=
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|
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ENST00000691421.1:c.1650T=
|
ENSP00000508674.1:p.Ala550=
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|
ENST00000691855.1:c.5971T=
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|
|
ENST00000692961.1:c.6429T=
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ENSP00000509289.1:p.Ala2143=
|
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ENST00000693677.1:c.705-619T=
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ENSP00000509779.1:n.705-619T=
|
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ENST00000420124.4:c.6429T=
MANE Select
|
ENSP00000398837.2:p.Ala2143=
|
|
ENST00000673918.1:c.6363T=
|
ENSP00000501283.1:p.Ala2121=
|
|
ENST00000674114.1:c.3751T=
|
|
|
ENST00000420124.2:c.6429T=
|
ENSP00000398837.1:p.Ala2143=
|
|
NM_014727.2:c.6429T=
|
NP_055542.1:p.Ala2143=
|
|
XM_011527561.1:c.6363T=
|
XP_011525863.1:p.Ala2121=
|
|
XM_011527562.1:c.6429T=
|
XP_011525864.1:p.Ala2143=
|
|
XM_011527563.1:c.6153T=
|
XP_011525865.1:p.Ala2051=
|
|
XM_011527561.2:c.5865T=
|
XP_011525863.2:p.Ala1955=
|
|
XM_011527562.2:c.6429T=
|
XP_011525864.1:p.Ala2143=
|
|
XM_017027544.1:c.6429T=
|
XP_016883033.1:p.Ala2143=
|
|
XM_017027545.1:c.5865T=
|
XP_016883034.1:p.Ala1955=
|
|
XM_017027546.1:c.3393T=
|
XP_016883035.1:p.Ala1131=
|
|
NM_014727.3:c.6429T=
MANE Select
|
NP_055542.1:p.Ala2143=
|
|