ENST00000506729.6:c.1853T>G
MANE Select
|
ENSP00000421339.1:p.Val618Gly
|
|
ENST00000379807.7:c.1853T>G
|
ENSP00000369135.3:p.Val618Gly
|
|
ENST00000389019.7:c.1667T>G
|
ENSP00000373671.3:p.Val556Gly
|
|
ENST00000506729.5:c.1853T>G
|
ENSP00000421339.1:p.Val618Gly
|
|
ENST00000513675.1:c.1094T>G
|
ENSP00000421990.1:p.Val365Gly
|
|
ENST00000514765.6:n.223T>G
|
|
|
NM_001289002.1:c.1853T>G
|
NP_001275931.1:p.Val618Gly
|
|
NM_001289004.1:c.1667T>G
|
NP_001275933.1:p.Val556Gly
|
|
NM_001308014.1:c.1094T>G
|
NP_001294943.1:p.Val365Gly
|
|
NM_173488.4:c.1853T>G
|
NP_775759.3:p.Val618Gly
|
|
XM_005271874.2:c.1853T>G
|
XP_005271931.1:p.Val618Gly
|
|
XM_011543147.1:c.1748T>G
|
XP_011541449.1:p.Val583Gly
|
|
XM_011543148.1:c.1616T>G
|
XP_011541450.1:p.Val539Gly
|
|
XM_011543149.1:c.1280T>G
|
XP_011541451.1:p.Val427Gly
|
|
XM_011543150.1:c.1124T>G
|
XP_011541452.1:p.Val375Gly
|
|
XM_011543151.1:c.1094T>G
|
XP_011541453.1:p.Val365Gly
|
|
XM_011543153.1:c.1031T>G
|
XP_011541455.1:p.Val344Gly
|
|
XM_005271874.3:c.1853T>G
|
XP_005271931.1:p.Val618Gly
|
|
XM_011543147.2:c.1748T>G
|
XP_011541449.1:p.Val583Gly
|
|
XM_011543148.2:c.1616T>G
|
XP_011541450.1:p.Val539Gly
|
|
XM_011543153.2:c.1031T>G
|
XP_011541455.1:p.Val344Gly
|
|
NM_001289002.2:c.1853T>G
|
NP_001275931.1:p.Val618Gly
|
|
NM_001289004.2:c.1667T>G
|
NP_001275933.1:p.Val556Gly
|
|
NM_001308014.2:c.1094T>G
|
NP_001294943.1:p.Val365Gly
|
|
NM_173488.5:c.1853T>G
MANE Select
|
NP_775759.3:p.Val618Gly
|
|