ENST00000682513.1:c.7841A>T
|
ENSP00000508201.1:p.Tyr2614Phe
|
|
ENST00000512123.4:c.7841A>T
MANE Select
|
ENSP00000422834.2:p.Tyr2614Phe
|
|
ENST00000512123.3:c.7841A>T
|
ENSP00000422834.2:p.Tyr2614Phe
|
|
NM_025074.6:c.7841A>T
|
NP_079350.5:p.Tyr2614Phe
|
|
XM_006714314.1:c.7835A>T
|
XP_006714377.1:p.Tyr2612Phe
|
|
XM_006714316.1:c.7613A>T
|
XP_006714379.1:p.Tyr2538Phe
|
|
XM_011532270.1:c.5540A>T
|
XP_011530572.1:p.Tyr1847Phe
|
|
XM_011532271.1:c.2729A>T
|
XP_011530573.1:p.Tyr910Phe
|
|
XM_006714316.3:c.7613A>T
|
XP_006714379.1:p.Tyr2538Phe
|
|
NM_025074.7:c.7841A>T
MANE Select
|
NP_079350.5:p.Tyr2614Phe
|
|