ENST00000347401.8:c.1229G>T
|
|
|
ENST00000353578.9:c.7966G>T
|
ENSP00000315873.4:p.Val2656Phe
|
|
ENST00000682957.1:c.711G>T
|
|
|
ENST00000684508.1:n.851G>T
|
|
|
ENST00000295550.9:c.8584G>T
MANE Select
|
ENSP00000295550.4:p.Val2862Phe
|
|
ENST00000295550.8:c.8584G>T
|
ENSP00000295550.4:p.Val2862Phe
|
|
ENST00000347401.7:c.6760G>T
|
ENSP00000315609.4:p.Val2254Phe
|
|
ENST00000353578.8:c.7966G>T
|
ENSP00000315873.4:p.Val2656Phe
|
|
ENST00000409809.5:c.7966G>T
|
ENSP00000386844.1:p.Val2656Phe
|
|
ENST00000472056.5:c.6763G>T
|
ENSP00000418285.1:p.Val2255Phe
|
|
ENST00000491769.1:n.5026G>T
|
|
|
NM_004369.3:c.8584G>T , LRG_473t1:c.8584G>T
|
NP_004360.2:p.Val2862Phe
|
|
NM_057166.4:c.6763G>T
|
NP_476507.3:p.Val2255Phe
|
|
NM_057167.3:c.7966G>T
|
NP_476508.2:p.Val2656Phe
|
|
XM_005246065.1:c.7984G>T
|
XP_005246122.1:p.Val2662Phe
|
|
XM_005246066.1:c.7363G>T
|
XP_005246123.1:p.Val2455Phe
|
|
XM_006712253.1:c.8083G>T
|
XP_006712316.1:p.Val2695Phe
|
|
XM_011510574.1:c.8581G>T
|
XP_011508876.1:p.Val2861Phe
|
|
XM_011510575.1:c.6178G>T
|
XP_011508877.1:p.Val2060Phe
|
|
XM_017003304.1:c.6178G>T
|
XP_016858793.1:p.Val2060Phe
|
|
XM_024452684.1:c.7363G>T
|
XP_024308452.1:p.Val2455Phe
|
|
NM_004369.4:c.8584G>T
MANE Select
|
NP_004360.2:p.Val2862Phe
|
|
NM_057166.5:c.6763G>T
|
NP_476507.3:p.Val2255Phe
|
|
NM_057167.4:c.7966G>T
|
NP_476508.2:p.Val2656Phe
|
|