|
NM_025074.7:c.8846A>T
MANE Select
|
NP_079350.5:p.Tyr2949Phe
|
|
ENST00000512123.4:c.8846A>T
MANE Select
|
ENSP00000422834.2:p.Tyr2949Phe
|
|
NM_025074.6:c.8846A>T
|
NP_079350.5:p.Tyr2949Phe
|
|
ENST00000512123.3:c.8846A>T
|
ENSP00000422834.2:p.Tyr2949Phe
|
|
ENST00000682513.1:c.8846A>T
|
ENSP00000508201.1:p.Tyr2949Phe
|
|
XM_006714314.1:c.8840A>T
|
XP_006714377.1:p.Tyr2947Phe
|
|
XM_006714316.1:c.8618A>T
|
XP_006714379.1:p.Tyr2873Phe
|
|
XM_006714316.3:c.8618A>T
|
XP_006714379.1:p.Tyr2873Phe
|
|
XM_011532270.1:c.6545A>T
|
XP_011530572.1:p.Tyr2182Phe
|
|
XM_011532271.1:c.3734A>T
|
XP_011530573.1:p.Tyr1245Phe
|