ENST00000347401.8:c.1497C>A
|
|
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ENST00000353578.9:c.8234C>A
|
ENSP00000315873.4:p.Ala2745Asp
|
|
ENST00000682957.1:c.979C>A
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|
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ENST00000684508.1:n.1119C>A
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|
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ENST00000295550.9:c.8852C>A
MANE Select
|
ENSP00000295550.4:p.Ala2951Asp
|
|
ENST00000295550.8:c.8852C>A
|
ENSP00000295550.4:p.Ala2951Asp
|
|
ENST00000347401.7:c.7028C>A
|
ENSP00000315609.4:p.Ala2343Asp
|
|
ENST00000353578.8:c.8234C>A
|
ENSP00000315873.4:p.Ala2745Asp
|
|
ENST00000409809.5:c.8234C>A
|
ENSP00000386844.1:p.Ala2745Asp
|
|
ENST00000472056.5:c.7031C>A
|
ENSP00000418285.1:p.Ala2344Asp
|
|
ENST00000491769.1:n.5294C>A
|
|
|
NM_004369.3:c.8852C>A , LRG_473t1:c.8852C>A
|
NP_004360.2:p.Ala2951Asp
|
|
NM_057166.4:c.7031C>A
|
NP_476507.3:p.Ala2344Asp
|
|
NM_057167.3:c.8234C>A
|
NP_476508.2:p.Ala2745Asp
|
|
XM_005246065.1:c.8252C>A
|
XP_005246122.1:p.Ala2751Asp
|
|
XM_005246066.1:c.7631C>A
|
XP_005246123.1:p.Ala2544Asp
|
|
XM_006712253.1:c.8351C>A
|
XP_006712316.1:p.Ala2784Asp
|
|
XM_011510574.1:c.8849C>A
|
XP_011508876.1:p.Ala2950Asp
|
|
XM_011510575.1:c.6446C>A
|
XP_011508877.1:p.Ala2149Asp
|
|
XM_017003304.1:c.6446C>A
|
XP_016858793.1:p.Ala2149Asp
|
|
XM_024452684.1:c.7631C>A
|
XP_024308452.1:p.Ala2544Asp
|
|
NM_004369.4:c.8852C>A
MANE Select
|
NP_004360.2:p.Ala2951Asp
|
|
NM_057166.5:c.7031C>A
|
NP_476507.3:p.Ala2344Asp
|
|
NM_057167.4:c.8234C>A
|
NP_476508.2:p.Ala2745Asp
|
|