ENST00000347401.8:c.1516T>C
|
|
|
ENST00000353578.9:c.8253T>C
|
ENSP00000315873.4:p.Ala2751=
|
|
ENST00000682957.1:c.998T>C
|
|
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ENST00000684508.1:n.1138T>C
|
|
|
ENST00000295550.9:c.8871T>C
MANE Select
|
ENSP00000295550.4:p.Ala2957=
|
|
ENST00000295550.8:c.8871T>C
|
ENSP00000295550.4:p.Ala2957=
|
|
ENST00000347401.7:c.7047T>C
|
ENSP00000315609.4:p.Ala2349=
|
|
ENST00000353578.8:c.8253T>C
|
ENSP00000315873.4:p.Ala2751=
|
|
ENST00000409809.5:c.8253T>C
|
ENSP00000386844.1:p.Ala2751=
|
|
ENST00000472056.5:c.7050T>C
|
ENSP00000418285.1:p.Ala2350=
|
|
ENST00000491769.1:n.5313T>C
|
|
|
NM_004369.3:c.8871T>C , LRG_473t1:c.8871T>C
|
NP_004360.2:p.Ala2957=
|
|
NM_057166.4:c.7050T>C
|
NP_476507.3:p.Ala2350=
|
|
NM_057167.3:c.8253T>C
|
NP_476508.2:p.Ala2751=
|
|
XM_005246065.1:c.8271T>C
|
XP_005246122.1:p.Ala2757=
|
|
XM_005246066.1:c.7650T>C
|
XP_005246123.1:p.Ala2550=
|
|
XM_006712253.1:c.8370T>C
|
XP_006712316.1:p.Ala2790=
|
|
XM_011510574.1:c.8868T>C
|
XP_011508876.1:p.Ala2956=
|
|
XM_011510575.1:c.6465T>C
|
XP_011508877.1:p.Ala2155=
|
|
XM_017003304.1:c.6465T>C
|
XP_016858793.1:p.Ala2155=
|
|
XM_024452684.1:c.7650T>C
|
XP_024308452.1:p.Ala2550=
|
|
NM_004369.4:c.8871T>C
MANE Select
|
NP_004360.2:p.Ala2957=
|
|
NM_057166.5:c.7050T>C
|
NP_476507.3:p.Ala2350=
|
|
NM_057167.4:c.8253T>C
|
NP_476508.2:p.Ala2751=
|
|