ENST00000347401.8:c.1019G>T
|
|
|
ENST00000353578.9:c.7756G>T
|
ENSP00000315873.4:p.Asp2586Tyr
|
|
ENST00000682957.1:c.377G>T
|
|
|
ENST00000684508.1:n.641G>T
|
|
|
ENST00000295550.9:c.8374G>T
MANE Select
|
ENSP00000295550.4:p.Asp2792Tyr
|
|
ENST00000295550.8:c.8374G>T
|
ENSP00000295550.4:p.Asp2792Tyr
|
|
ENST00000347401.7:c.6550G>T
|
ENSP00000315609.4:p.Asp2184Tyr
|
|
ENST00000353578.8:c.7756G>T
|
ENSP00000315873.4:p.Asp2586Tyr
|
|
ENST00000409809.5:c.7756G>T
|
ENSP00000386844.1:p.Asp2586Tyr
|
|
ENST00000468792.1:n.61G>T
|
|
|
ENST00000472056.5:c.6553G>T
|
ENSP00000418285.1:p.Asp2185Tyr
|
|
ENST00000491769.1:n.4816G>T
|
|
|
NM_004369.3:c.8374G>T , LRG_473t1:c.8374G>T
|
NP_004360.2:p.Asp2792Tyr
|
|
NM_057166.4:c.6553G>T
|
NP_476507.3:p.Asp2185Tyr
|
|
NM_057167.3:c.7756G>T
|
NP_476508.2:p.Asp2586Tyr
|
|
XM_005246065.1:c.7774G>T
|
XP_005246122.1:p.Asp2592Tyr
|
|
XM_005246066.1:c.7153G>T
|
XP_005246123.1:p.Asp2385Tyr
|
|
XM_006712253.1:c.7873G>T
|
XP_006712316.1:p.Asp2625Tyr
|
|
XM_011510574.1:c.8371G>T
|
XP_011508876.1:p.Asp2791Tyr
|
|
XM_011510575.1:c.5968G>T
|
XP_011508877.1:p.Asp1990Tyr
|
|
XM_017003304.1:c.5968G>T
|
XP_016858793.1:p.Asp1990Tyr
|
|
XM_024452684.1:c.7153G>T
|
XP_024308452.1:p.Asp2385Tyr
|
|
NM_004369.4:c.8374G>T
MANE Select
|
NP_004360.2:p.Asp2792Tyr
|
|
NM_057166.5:c.6553G>T
|
NP_476507.3:p.Asp2185Tyr
|
|
NM_057167.4:c.7756G>T
|
NP_476508.2:p.Asp2586Tyr
|
|