ENST00000597188.6:c.3252T=
MANE Select
|
ENSP00000471851.1:p.Phe1084=
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|
ENST00000270328.8:c.3252T=
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ENSP00000270328.4:p.Phe1084=
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|
ENST00000593913.5:c.*2129T=
|
ENSP00000469901.1:n.*2129T=
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|
ENST00000595838.5:c.1713T=
|
ENSP00000470501.1:p.Phe571=
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|
ENST00000597188.5:c.3252T=
|
ENSP00000471851.1:p.Phe1084=
|
|
NM_001282352.1:c.1713T=
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NP_001269281.1:p.Phe571=
|
|
NM_030957.3:c.3252T=
|
NP_112219.3:p.Phe1084=
|
|
XM_006722917.2:c.2295T=
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XP_006722980.1:p.Phe765=
|
|
XM_011528331.1:c.3399T=
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XP_011526633.1:p.Phe1133=
|
|
XM_011528332.1:c.3399T=
|
XP_011526634.1:p.Phe1133=
|
|
XM_011528333.1:c.3399T=
|
XP_011526635.1:p.Phe1133=
|
|
XM_011528334.1:c.3075T=
|
XP_011526636.1:p.Phe1025=
|
|
XM_011528335.1:c.1968T=
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XP_011526637.1:p.Phe656=
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|
XM_011528336.1:c.1962T=
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XP_011526638.1:p.Phe654=
|
|
XM_006722917.3:c.2295T=
|
XP_006722980.1:p.Phe765=
|
|
XM_017027338.2:c.3252T=
|
XP_016882827.1:p.Phe1084=
|
|
XM_017027339.1:c.1821T=
|
XP_016882828.1:p.Phe607=
|
|
XM_017027340.1:c.1815T=
|
XP_016882829.1:p.Phe605=
|
|
NM_030957.4:c.3252T=
MANE Select
|
NP_112219.3:p.Phe1084=
|
|
NM_001282352.2:c.1713T=
|
NP_001269281.1:p.Phe571=
|
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