ENST00000233575.7:c.806A>T
MANE Select
|
ENSP00000233575.2:p.Tyr269Phe
|
|
ENST00000233575.6:c.806A>T
|
ENSP00000233575.2:p.Tyr269Phe
|
|
ENST00000427123.5:c.*616A>T
|
ENSP00000405399.1:n.*616A>T
|
|
ENST00000440760.5:c.*651A>T
|
ENSP00000399727.1:n.*651A>T
|
|
ENST00000453453.1:c.*333A>T
|
ENSP00000401922.1:n.*333A>T
|
|
ENST00000493711.1:n.523A>T
|
|
|
ENST00000537606.5:c.731A>T
|
ENSP00000439208.1:p.Tyr244Phe
|
|
NM_001267059.1:c.770A>T
|
NP_001253988.1:p.Tyr257Phe
|
|
NM_001267060.1:c.731A>T
|
NP_001253989.1:p.Tyr244Phe
|
|
NM_001267061.1:c.746A>T
|
NP_001253990.1:p.Tyr249Phe
|
|
NM_014748.3:c.806A>T
|
NP_055563.1:p.Tyr269Phe
|
|
NR_049782.1:n.1179A>T
|
|
|
NR_049783.1:n.1152A>T
|
|
|
NR_049784.1:n.1128A>T
|
|
|
NR_049785.1:n.1061A>T
|
|
|
NR_049786.1:n.1010A>T
|
|
|
NR_049787.1:n.861A>T
|
|
|
NR_049788.1:n.791A>T
|
|
|
XM_011533203.1:c.164A>T
|
XP_011531505.1:p.Tyr55Phe
|
|
XM_011533203.2:c.164A>T
|
XP_011531505.1:p.Tyr55Phe
|
|
XM_017005405.2:c.164A>T
|
XP_016860894.1:p.Tyr55Phe
|
|
NM_014748.4:c.806A>T
MANE Select
|
NP_055563.1:p.Tyr269Phe
|
|
NM_001267059.2:c.770A>T
|
NP_001253988.1:p.Tyr257Phe
|
|
NM_001267061.2:c.746A>T
|
NP_001253990.1:p.Tyr249Phe
|
|
NR_049782.2:n.1059A>T
|
|
|
NR_049783.2:n.1032A>T
|
|
|
NR_049784.2:n.1008A>T
|
|
|
NR_049785.2:n.941A>T
|
|
|
NR_049786.2:n.890A>T
|
|
|
NR_049787.2:n.741A>T
|
|
|
NR_049788.2:n.671A>T
|
|
|
NM_001267060.2:c.731A>T
|
NP_001253989.1:p.Tyr244Phe
|
|