|
ENST00000394904.9:c.1246A>G
|
ENSP00000378364.3:p.Thr416Ala
|
|
|
ENST00000545993.7:c.1147A>G
|
ENSP00000442810.2:p.Thr383Ala
|
|
|
ENST00000547688.7:c.1246A>G
|
ENSP00000449200.2:p.Thr416Ala
|
|
|
ENST00000642227.1:c.*744A>G
|
ENSP00000494696.1:n.*744A>G
|
|
|
ENST00000643123.1:n.211A>G
|
|
|
|
ENST00000643884.1:c.1195A>G
|
ENSP00000493633.1:p.Thr399Ala
|
|
|
ENST00000644495.1:c.1159A>G
|
ENSP00000494107.1:p.Thr387Ala
|
|
|
ENST00000646264.1:c.729A>G
|
|
|
|
ENST00000646740.1:c.*333A>G
|
ENSP00000494001.1:n.*333A>G
|
|
|
ENST00000262051.11:c.1159A>G
|
ENSP00000262051.7:p.Thr387Ala
|
|
|
ENST00000262052.9:c.1159A>G
MANE Select
|
ENSP00000262052.5:p.Thr387Ala
|
|
|
ENST00000394904.7:c.1246A>G
|
ENSP00000378364.3:p.Thr416Ala
|
|
|
ENST00000541174.6:c.1159A>G
|
ENSP00000444542.2:p.Thr387Ala
|
|
|
ENST00000545993.6:c.1147A>G
|
ENSP00000442810.2:p.Thr383Ala
|
|
|
ENST00000546636.5:c.1159A>G
|
ENSP00000449008.1:p.Thr387Ala
|
|
|
ENST00000546743.5:c.922A>G
|
ENSP00000446914.1:p.Thr308Ala
|
|
|
ENST00000547198.5:c.1159A>G
|
ENSP00000446769.1:p.Thr387Ala
|
|
|
ENST00000547688.5:c.1246A>G
|
ENSP00000449200.1:p.Thr416Ala
|
|
|
ENST00000550782.5:n.631A>G
|
|
|
|
ENST00000551231.1:n.297A>G
|
|
|
|
NM_000617.2:c.1159A>G
|
NP_000608.1:p.Thr387Ala
|
|
|
NM_001174125.1:c.1246A>G
|
NP_001167596.1:p.Thr416Ala
|
|
|
NM_001174126.1:c.1159A>G
|
NP_001167597.1:p.Thr387Ala
|
|
|
NM_001174127.1:c.1159A>G
|
NP_001167598.1:p.Thr387Ala
|
|
|
NM_001174128.1:c.1159A>G
|
NP_001167599.1:p.Thr387Ala
|
|
|
NM_001174129.1:c.1159A>G
|
NP_001167600.1:p.Thr387Ala
|
|
|
NM_001174130.1:c.1147A>G
|
NP_001167601.1:p.Thr383Ala
|
|
|
NR_033421.1:n.1224A>G
|
|
|
|
NR_033422.1:n.1299A>G
|
|
|
|
XM_005268911.2:c.1246A>G
|
XP_005268968.1:p.Thr416Ala
|
|
|
XM_005268912.3:c.1147A>G
|
XP_005268969.1:p.Thr383Ala
|
|
|
XM_005268913.2:c.1048A>G
|
XP_005268970.1:p.Thr350Ala
|
|
|
XM_005268914.2:c.1048A>G
|
XP_005268971.1:p.Thr350Ala
|
|
|
XM_011538404.1:c.1159A>G
|
XP_011536706.1:p.Thr387Ala
|
|
|
XM_011538405.1:c.1159A>G
|
XP_011536707.1:p.Thr387Ala
|
|
|
XM_011538406.1:c.922A>G
|
XP_011536708.1:p.Thr308Ala
|
|
|
XR_429104.1:n.1356A>G
|
|
|
|
XR_944555.1:n.1356A>G
|
|
|
|
XM_005268911.3:c.1246A>G
|
XP_005268968.1:p.Thr416Ala
|
|
|
XM_005268912.5:c.1147A>G
|
XP_005268969.1:p.Thr383Ala
|
|
|
XM_011538404.3:c.1159A>G
|
XP_011536706.1:p.Thr387Ala
|
|
|
XM_011538405.3:c.1159A>G
|
XP_011536707.1:p.Thr387Ala
|
|
|
XM_017019355.2:c.1159A>G
|
XP_016874844.1:p.Thr387Ala
|
|
|
XM_017019356.2:c.922A>G
|
XP_016874845.1:p.Thr308Ala
|
|
|
XR_001748720.1:n.1356A>G
|
|
|
|
XR_001748721.2:n.1274A>G
|
|
|
|
XR_001748722.2:n.1282A>G
|
|
|
|
XR_001748723.2:n.1282A>G
|
|
|
|
NM_000617.3:c.1159A>G
MANE Select
|
NP_000608.1:p.Thr387Ala
|
|
|
NM_001174125.2:c.1246A>G
|
NP_001167596.1:p.Thr416Ala
|
|
|
NM_001174128.2:c.1159A>G
|
NP_001167599.1:p.Thr387Ala
|
|
|
NM_001174130.2:c.1147A>G
|
NP_001167601.1:p.Thr383Ala
|
|
|
NR_033421.2:n.1192A>G
|
|
|
|
NR_033422.2:n.1267A>G
|
|
|
|
NM_001174126.2:c.1159A>G
|
NP_001167597.1:p.Thr387Ala
|
|
|
NM_001174127.2:c.1159A>G
|
NP_001167598.1:p.Thr387Ala
|
|
|
NM_001379446.1:c.1246A>G
|
NP_001366375.1:p.Thr416Ala
|
|
|
NM_001379447.1:c.1159A>G
|
NP_001366376.1:p.Thr387Ala
|
|
|
NM_001379448.1:c.1147A>G
|
NP_001366377.1:p.Thr383Ala
|
|
|
NM_001379455.1:c.1246A>G
|
NP_001366384.1:p.Thr416Ala
|
|
|
NR_166668.1:n.1272A>G
|
|
|
|
NR_166669.1:n.1267A>G
|
|
|
|
NR_166670.1:n.1272A>G
|
|
|
