ENST00000347401.8:c.1016A>C
|
|
|
ENST00000353578.9:c.7753A>C
|
ENSP00000315873.4:p.Asn2585His
|
|
ENST00000682957.1:c.374A>C
|
|
|
ENST00000684508.1:n.638A>C
|
|
|
ENST00000295550.9:c.8371A>C
MANE Select
|
ENSP00000295550.4:p.Asn2791His
|
|
ENST00000295550.8:c.8371A>C
|
ENSP00000295550.4:p.Asn2791His
|
|
ENST00000347401.7:c.6547A>C
|
ENSP00000315609.4:p.Asn2183His
|
|
ENST00000353578.8:c.7753A>C
|
ENSP00000315873.4:p.Asn2585His
|
|
ENST00000409809.5:c.7753A>C
|
ENSP00000386844.1:p.Asn2585His
|
|
ENST00000468792.1:n.58A>C
|
|
|
ENST00000472056.5:c.6550A>C
|
ENSP00000418285.1:p.Asn2184His
|
|
ENST00000491769.1:n.4813A>C
|
|
|
NM_004369.3:c.8371A>C , LRG_473t1:c.8371A>C
|
NP_004360.2:p.Asn2791His
|
|
NM_057166.4:c.6550A>C
|
NP_476507.3:p.Asn2184His
|
|
NM_057167.3:c.7753A>C
|
NP_476508.2:p.Asn2585His
|
|
XM_005246065.1:c.7771A>C
|
XP_005246122.1:p.Asn2591His
|
|
XM_005246066.1:c.7150A>C
|
XP_005246123.1:p.Asn2384His
|
|
XM_006712253.1:c.7870A>C
|
XP_006712316.1:p.Asn2624His
|
|
XM_011510574.1:c.8368A>C
|
XP_011508876.1:p.Asn2790His
|
|
XM_011510575.1:c.5965A>C
|
XP_011508877.1:p.Asn1989His
|
|
XM_017003304.1:c.5965A>C
|
XP_016858793.1:p.Asn1989His
|
|
XM_024452684.1:c.7150A>C
|
XP_024308452.1:p.Asn2384His
|
|
NM_004369.4:c.8371A>C
MANE Select
|
NP_004360.2:p.Asn2791His
|
|
NM_057166.5:c.6550A>C
|
NP_476507.3:p.Asn2184His
|
|
NM_057167.4:c.7753A>C
|
NP_476508.2:p.Asn2585His
|
|