ENST00000347401.8:c.115C>A
|
|
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ENST00000353578.9:c.6852C>A
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ENSP00000315873.4:p.Ala2284=
|
|
ENST00000295550.9:c.7470C>A
MANE Select
|
ENSP00000295550.4:p.Ala2490=
|
|
ENST00000295550.8:c.7470C>A
|
ENSP00000295550.4:p.Ala2490=
|
|
ENST00000347401.7:c.5646C>A
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ENSP00000315609.4:p.Ala1882=
|
|
ENST00000353578.8:c.6852C>A
|
ENSP00000315873.4:p.Ala2284=
|
|
ENST00000409809.5:c.6852C>A
|
ENSP00000386844.1:p.Ala2284=
|
|
ENST00000472056.5:c.5649C>A
|
ENSP00000418285.1:p.Ala1883=
|
|
ENST00000491769.1:n.1724C>A
|
|
|
NM_004369.3:c.7470C>A , LRG_473t1:c.7470C>A
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NP_004360.2:p.Ala2490=
|
|
NM_057166.4:c.5649C>A
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NP_476507.3:p.Ala1883=
|
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NM_057167.3:c.6852C>A
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NP_476508.2:p.Ala2284=
|
|
XM_005246065.1:c.6870C>A
|
XP_005246122.1:p.Ala2290=
|
|
XM_005246066.1:c.6249C>A
|
XP_005246123.1:p.Ala2083=
|
|
XM_006712253.1:c.6969C>A
|
XP_006712316.1:p.Ala2323=
|
|
XM_011510574.1:c.7467C>A
|
XP_011508876.1:p.Ala2489=
|
|
XM_011510575.1:c.5064C>A
|
XP_011508877.1:p.Ala1688=
|
|
XM_017003304.1:c.5064C>A
|
XP_016858793.1:p.Ala1688=
|
|
XM_024452684.1:c.6249C>A
|
XP_024308452.1:p.Ala2083=
|
|
NM_004369.4:c.7470C>A
MANE Select
|
NP_004360.2:p.Ala2490=
|
|
NM_057166.5:c.5649C>A
|
NP_476507.3:p.Ala1883=
|
|
NM_057167.4:c.6852C>A
|
NP_476508.2:p.Ala2284=
|
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