ENST00000299314.12:c.2676G>T
MANE Select
|
ENSP00000299314.7:p.Leu892Phe
|
|
ENST00000299314.11:c.2676G>T
|
ENSP00000299314.7:p.Leu892Phe
|
|
NM_024312.4:c.2676G>T
|
NP_077288.2:p.Leu892Phe
|
|
XM_006719593.2:c.2676G>T
|
XP_006719656.1:p.Leu892Phe
|
|
XM_011538731.1:c.2595G>T
|
XP_011537033.1:p.Leu865Phe
|
|
XM_006719593.3:c.2676G>T
|
XP_006719656.1:p.Leu892Phe
|
|
XM_011538731.2:c.2595G>T
|
XP_011537033.1:p.Leu865Phe
|
|
XM_017019961.1:c.2460G>T
|
XP_016875450.1:p.Leu820Phe
|
|
XM_017019962.2:c.1449G>T
|
XP_016875451.1:p.Leu483Phe
|
|
NM_024312.5:c.2676G>T
MANE Select
|
NP_077288.2:p.Leu892Phe
|
|