ENST00000261769.10:c.1460T>C
MANE Select
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ENSP00000261769.4:p.Val487Ala
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|
ENST00000261769.9:c.1460T>C
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ENSP00000261769.4:p.Val487Ala
|
|
ENST00000422392.6:c.1277T>C
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ENSP00000414946.2:p.Val426Ala
|
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ENST00000562836.5:n.1531T>C
|
|
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ENST00000566510.5:c.*126T>C
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ENSP00000458139.1:n.*126T>C
|
|
ENST00000566612.5:c.1460T>C
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ENSP00000454782.1:p.Val487Ala
|
|
ENST00000611625.4:c.1523T>C
|
ENSP00000481063.1:p.Val508Ala
|
|
ENST00000612417.4:c.1460T>C
|
ENSP00000478360.1:p.Val487Ala
|
|
ENST00000621016.4:c.1460T>C
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ENSP00000480664.1:p.Val487Ala
|
|
NM_004360.3:c.1460T>C , LRG_301t1:c.1460T>C
|
NP_004351.1:p.Val487Ala
|
|
XM_011523488.1:c.725T>C
|
XP_011521790.1:p.Val242Ala
|
|
XM_011523489.1:c.725T>C
|
XP_011521791.1:p.Val242Ala
|
|
NM_001317184.1:c.1277T>C
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NP_001304113.1:p.Val426Ala
|
|
NM_001317185.1:c.-89T>C
|
NP_001304114.1:n.-89T>C
|
|
NM_001317186.1:c.-360T>C
|
NP_001304115.1:n.-360T>C
|
|
NM_004360.4:c.1460T>C
|
NP_004351.1:p.Val487Ala
|
|
NM_004360.5:c.1460T>C
MANE Select
|
NP_004351.1:p.Val487Ala
|
|
NM_001317184.2:c.1277T>C
|
NP_001304113.1:p.Val426Ala
|
|
NM_001317185.2:c.-89T>C
|
NP_001304114.1:n.-89T>C
|
|
NM_001317186.2:c.-360T>C
|
NP_001304115.1:n.-360T>C
|
|