ENST00000347401.8:c.1349C>G
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ENST00000353578.9:c.8086C>G
|
ENSP00000315873.4:p.Gln2696Glu
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ENST00000682957.1:c.831C>G
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ENST00000684508.1:n.971C>G
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ENST00000295550.9:c.8704C>G
MANE Select
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ENSP00000295550.4:p.Gln2902Glu
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ENST00000295550.8:c.8704C>G
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ENSP00000295550.4:p.Gln2902Glu
|
|
ENST00000347401.7:c.6880C>G
|
ENSP00000315609.4:p.Gln2294Glu
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|
ENST00000353578.8:c.8086C>G
|
ENSP00000315873.4:p.Gln2696Glu
|
|
ENST00000409809.5:c.8086C>G
|
ENSP00000386844.1:p.Gln2696Glu
|
|
ENST00000472056.5:c.6883C>G
|
ENSP00000418285.1:p.Gln2295Glu
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ENST00000491769.1:n.5146C>G
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|
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NM_004369.3:c.8704C>G , LRG_473t1:c.8704C>G
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NP_004360.2:p.Gln2902Glu
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NM_057166.4:c.6883C>G
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NP_476507.3:p.Gln2295Glu
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|
NM_057167.3:c.8086C>G
|
NP_476508.2:p.Gln2696Glu
|
|
XM_005246065.1:c.8104C>G
|
XP_005246122.1:p.Gln2702Glu
|
|
XM_005246066.1:c.7483C>G
|
XP_005246123.1:p.Gln2495Glu
|
|
XM_006712253.1:c.8203C>G
|
XP_006712316.1:p.Gln2735Glu
|
|
XM_011510574.1:c.8701C>G
|
XP_011508876.1:p.Gln2901Glu
|
|
XM_011510575.1:c.6298C>G
|
XP_011508877.1:p.Gln2100Glu
|
|
XM_017003304.1:c.6298C>G
|
XP_016858793.1:p.Gln2100Glu
|
|
XM_024452684.1:c.7483C>G
|
XP_024308452.1:p.Gln2495Glu
|
|
NM_004369.4:c.8704C>G
MANE Select
|
NP_004360.2:p.Gln2902Glu
|
|
NM_057166.5:c.6883C>G
|
NP_476507.3:p.Gln2295Glu
|
|
NM_057167.4:c.8086C>G
|
NP_476508.2:p.Gln2696Glu
|
|