ENST00000236671.7:c.940G>T
MANE Select
|
ENSP00000236671.2:p.Ala314Ser
|
|
ENST00000367196.4:c.835G>T
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ENSP00000356164.4:p.Ala279Ser
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ENST00000427721.3:c.365G>T
|
|
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ENST00000429746.2:c.835G>T
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ENSP00000402586.2:p.Ala279Ser
|
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ENST00000433655.6:c.*106G>T
|
ENSP00000404902.1:n.*106G>T
|
|
ENST00000438213.6:c.1057G>T
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ENSP00000415036.2:p.Ala353Ser
|
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ENST00000497544.3:n.556G>T
|
|
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ENST00000636397.1:c.940G>T
|
ENSP00000489910.1:p.Ala314Ser
|
|
ENST00000636571.1:c.919G>T
|
ENSP00000490770.1:p.Ala307Ser
|
|
ENST00000636615.1:c.940G>T
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ENSP00000490014.1:p.Ala314Ser
|
|
ENST00000636843.1:c.934G>T
|
ENSP00000490897.1:p.Ala312Ser
|
|
ENST00000637158.1:n.538G>T
|
|
|
ENST00000637381.2:n.3368G>T
|
|
|
ENST00000637387.1:c.940G>T
|
ENSP00000490598.1:p.Ala314Ser
|
|
ENST00000637815.2:c.922G>T
|
ENSP00000490344.1:p.Ala308Ser
|
|
ENST00000637915.1:c.940G>T
|
ENSP00000490471.1:p.Ala314Ser
|
|
ENST00000637937.1:n.248G>T
|
|
|
ENST00000678991.1:c.*801G>T
|
ENSP00000503019.1:n.*801G>T
|
|
ENST00000236671.6:c.940G>T
|
ENSP00000236671.2:p.Ala314Ser
|
|
ENST00000427721.2:c.340G>T
|
ENSP00000415840.2:p.Ala114Ser
|
|
ENST00000429746.1:c.271G>T
|
ENSP00000402586.1:p.Ala91Ser
|
|
ENST00000433655.5:c.*106G>T
|
ENSP00000404902.1:n.*106G>T
|
|
ENST00000438213.5:c.895G>T
|
ENSP00000415036.1:p.Ala299Ser
|
|
ENST00000497544.1:n.556G>T
|
|
|
NM_001909.4:c.940G>T
|
NP_001900.1:p.Ala314Ser
|
|
NM_001909.5:c.940G>T
MANE Select
|
NP_001900.1:p.Ala314Ser
|
|