ENST00000347401.8:c.295G=
|
|
|
ENST00000353578.9:c.7032G=
|
ENSP00000315873.4:p.Gln2344=
|
|
ENST00000295550.9:c.7650G=
MANE Select
|
ENSP00000295550.4:p.Gln2550=
|
|
ENST00000295550.8:c.7650G=
|
ENSP00000295550.4:p.Gln2550=
|
|
ENST00000347401.7:c.5826G=
|
ENSP00000315609.4:p.Gln1942=
|
|
ENST00000353578.8:c.7032G=
|
ENSP00000315873.4:p.Gln2344=
|
|
ENST00000409809.5:c.7032G=
|
ENSP00000386844.1:p.Gln2344=
|
|
ENST00000472056.5:c.5829G=
|
ENSP00000418285.1:p.Gln1943=
|
|
ENST00000491769.1:n.1904G=
|
|
|
NM_004369.3:c.7650G= , LRG_473t1:c.7650G=
|
NP_004360.2:p.Gln2550=
|
|
NM_057166.4:c.5829G=
|
NP_476507.3:p.Gln1943=
|
|
NM_057167.3:c.7032G=
|
NP_476508.2:p.Gln2344=
|
|
XM_005246065.1:c.7050G=
|
XP_005246122.1:p.Gln2350=
|
|
XM_005246066.1:c.6429G=
|
XP_005246123.1:p.Gln2143=
|
|
XM_006712253.1:c.7149G=
|
XP_006712316.1:p.Gln2383=
|
|
XM_011510574.1:c.7647G=
|
XP_011508876.1:p.Gln2549=
|
|
XM_011510575.1:c.5244G=
|
XP_011508877.1:p.Gln1748=
|
|
XM_017003304.1:c.5244G=
|
XP_016858793.1:p.Gln1748=
|
|
XM_024452684.1:c.6429G=
|
XP_024308452.1:p.Gln2143=
|
|
NM_004369.4:c.7650G=
MANE Select
|
NP_004360.2:p.Gln2550=
|
|
NM_057166.5:c.5829G=
|
NP_476507.3:p.Gln1943=
|
|
NM_057167.4:c.7032G=
|
NP_476508.2:p.Gln2344=
|
|