ENST00000347401.8:c.1023T>G
|
|
|
ENST00000353578.9:c.7760T>G
|
ENSP00000315873.4:p.Val2587Gly
|
|
ENST00000682957.1:c.381T>G
|
|
|
ENST00000684508.1:n.645T>G
|
|
|
ENST00000295550.9:c.8378T>G
MANE Select
|
ENSP00000295550.4:p.Val2793Gly
|
|
ENST00000295550.8:c.8378T>G
|
ENSP00000295550.4:p.Val2793Gly
|
|
ENST00000347401.7:c.6554T>G
|
ENSP00000315609.4:p.Val2185Gly
|
|
ENST00000353578.8:c.7760T>G
|
ENSP00000315873.4:p.Val2587Gly
|
|
ENST00000409809.5:c.7760T>G
|
ENSP00000386844.1:p.Val2587Gly
|
|
ENST00000468792.1:n.65T>G
|
|
|
ENST00000472056.5:c.6557T>G
|
ENSP00000418285.1:p.Val2186Gly
|
|
ENST00000491769.1:n.4820T>G
|
|
|
NM_004369.3:c.8378T>G , LRG_473t1:c.8378T>G
|
NP_004360.2:p.Val2793Gly
|
|
NM_057166.4:c.6557T>G
|
NP_476507.3:p.Val2186Gly
|
|
NM_057167.3:c.7760T>G
|
NP_476508.2:p.Val2587Gly
|
|
XM_005246065.1:c.7778T>G
|
XP_005246122.1:p.Val2593Gly
|
|
XM_005246066.1:c.7157T>G
|
XP_005246123.1:p.Val2386Gly
|
|
XM_006712253.1:c.7877T>G
|
XP_006712316.1:p.Val2626Gly
|
|
XM_011510574.1:c.8375T>G
|
XP_011508876.1:p.Val2792Gly
|
|
XM_011510575.1:c.5972T>G
|
XP_011508877.1:p.Val1991Gly
|
|
XM_017003304.1:c.5972T>G
|
XP_016858793.1:p.Val1991Gly
|
|
XM_024452684.1:c.7157T>G
|
XP_024308452.1:p.Val2386Gly
|
|
NM_004369.4:c.8378T>G
MANE Select
|
NP_004360.2:p.Val2793Gly
|
|
NM_057166.5:c.6557T>G
|
NP_476507.3:p.Val2186Gly
|
|
NM_057167.4:c.7760T>G
|
NP_476508.2:p.Val2587Gly
|
|