ENST00000260197.12:c.3563A>T
MANE Select
|
ENSP00000260197.6:p.Asp1188Val
|
|
ENST00000260197.11:c.3563A>T
|
ENSP00000260197.6:p.Asp1188Val
|
|
ENST00000525532.5:c.395A>T
|
ENSP00000434634.1:p.Asp132Val
|
|
ENST00000532694.5:c.101A>T
|
ENSP00000432131.1:p.Asp34Val
|
|
ENST00000534286.5:c.293A>T
|
ENSP00000436447.1:p.Asp98Val
|
|
NM_003105.5:c.3563A>T
|
NP_003096.1:p.Asp1188Val
|
|
XM_011542963.1:c.3449A>T
|
XP_011541265.1:p.Asp1150Val
|
|
XM_011542964.1:c.3563A>T
|
XP_011541266.1:p.Asp1188Val
|
|
XM_011542965.1:c.2024A>T
|
XP_011541267.1:p.Asp675Val
|
|
XM_011542966.1:c.923A>T
|
XP_011541268.1:p.Asp308Val
|
|
XM_011542967.1:c.395A>T
|
XP_011541269.1:p.Asp132Val
|
|
XM_011542963.3:c.3449A>T
|
XP_011541265.1:p.Asp1150Val
|
|
XM_011542965.3:c.2024A>T
|
XP_011541267.1:p.Asp675Val
|
|
XM_011542967.3:c.395A>T
|
XP_011541269.1:p.Asp132Val
|
|
XM_017018169.2:c.3251A>T
|
XP_016873658.1:p.Asp1084Val
|
|
XM_017018170.2:c.3038A>T
|
XP_016873659.1:p.Asp1013Val
|
|
XM_017018171.1:c.3563A>T
|
XP_016873660.1:p.Asp1188Val
|
|
XM_017018172.2:c.923A>T
|
XP_016873661.1:p.Asp308Val
|
|
NM_003105.6:c.3563A>T
MANE Select
|
NP_003096.2:p.Asp1188Val
|
|