ENST00000597188.6:c.3310T>G
MANE Select
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ENSP00000471851.1:p.Ter1104Glu
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ENST00000270328.8:c.3310T>G
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ENSP00000270328.4:p.Ter1104Glu
|
|
ENST00000593913.5:c.*2187T>G
|
ENSP00000469901.1:n.*2187T>G
|
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ENST00000595838.5:c.1771T>G
|
ENSP00000470501.1:p.Ter591Glu
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ENST00000597188.5:c.3310T>G
|
ENSP00000471851.1:p.Ter1104Glu
|
|
NM_001282352.1:c.1771T>G
|
NP_001269281.1:p.Ter591Glu
|
|
NM_030957.3:c.3310T>G
|
NP_112219.3:p.Ter1104Glu
|
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XM_006722917.2:c.2353T>G
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XP_006722980.1:p.Ter785Glu
|
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XM_011528331.1:c.3457T>G
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XP_011526633.1:p.Ter1153Glu
|
|
XM_011528332.1:c.3457T>G
|
XP_011526634.1:p.Ter1153Glu
|
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XM_011528333.1:c.3457T>G
|
XP_011526635.1:p.Ter1153Glu
|
|
XM_011528334.1:c.3133T>G
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XP_011526636.1:p.Ter1045Glu
|
|
XM_011528335.1:c.2026T>G
|
XP_011526637.1:p.Ter676Glu
|
|
XM_011528336.1:c.2020T>G
|
XP_011526638.1:p.Ter674Glu
|
|
XM_006722917.3:c.2353T>G
|
XP_006722980.1:p.Ter785Glu
|
|
XM_017027338.2:c.3310T>G
|
XP_016882827.1:p.Ter1104Glu
|
|
XM_017027339.1:c.1879T>G
|
XP_016882828.1:p.Ter627Glu
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|
XM_017027340.1:c.1873T>G
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XP_016882829.1:p.Ter625Glu
|
|
NM_030957.4:c.3310T>G
MANE Select
|
NP_112219.3:p.Ter1104Glu
|
|
NM_001282352.2:c.1771T>G
|
NP_001269281.1:p.Ter591Glu
|
|