ENST00000367400.8:c.2385G>T
MANE Select
|
ENSP00000356370.3:p.Leu795Phe
|
|
ENST00000638467.1:c.2385G>T
|
ENSP00000491102.1:p.Leu795Phe
|
|
ENST00000681519.1:c.1266G>T
|
ENSP00000505267.1:p.Leu422Phe
|
|
ENST00000367397.1:c.528G>T
|
ENSP00000356367.1:p.Leu176Phe
|
|
ENST00000367399.6:c.2049G>T
|
ENSP00000356369.2:p.Leu683Phe
|
|
ENST00000367400.7:c.2385G>T
|
ENSP00000356370.3:p.Leu795Phe
|
|
ENST00000480086.2:n.286G>T
|
|
|
ENST00000484075.5:c.2385G>T
|
ENSP00000433932.1:p.Leu795Phe
|
|
ENST00000535699.5:c.2178G>T
|
ENSP00000438786.1:p.Leu726Phe
|
|
ENST00000538660.5:c.2128+5754G>T
|
ENSP00000438091.1:n.2128+5754G>T
|
|
NM_001193640.1:c.2049G>T
|
NP_001180569.1:p.Leu683Phe
|
|
NM_001257965.1:c.2178G>T
|
NP_001244894.1:p.Leu726Phe
|
|
NM_001257966.1:c.2128+5754G>T
|
NP_001244895.1:n.2128+5754G>T
|
|
NM_201253.2:c.2385G>T
|
NP_957705.1:p.Leu795Phe
|
|
NR_047563.1:n.2386G>T
|
|
|
NR_047564.1:n.2594G>T
|
|
|
XM_011509365.1:c.2385G>T
|
XP_011507667.1:p.Leu795Phe
|
|
XM_011509366.1:c.2385G>T
|
XP_011507668.1:p.Leu795Phe
|
|
XM_011509367.1:c.2385G>T
|
XP_011507669.1:p.Leu795Phe
|
|
XM_011509368.1:c.1803G>T
|
XP_011507670.1:p.Leu601Phe
|
|
XM_011509369.1:c.828G>T
|
XP_011507671.1:p.Leu276Phe
|
|
XM_011509365.2:c.2385G>T
|
XP_011507667.1:p.Leu795Phe
|
|
XM_011509369.2:c.828G>T
|
XP_011507671.1:p.Leu276Phe
|
|
XM_017000851.1:c.1542G>T
|
XP_016856340.1:p.Leu514Phe
|
|
XM_017000852.1:c.2385G>T
|
XP_016856341.1:p.Leu795Phe
|
|
NM_201253.3:c.2385G>T
MANE Select
|
NP_957705.1:p.Leu795Phe
|
|
NM_001193640.2:c.2049G>T
|
NP_001180569.1:p.Leu683Phe
|
|
NM_001257965.2:c.2178G>T
|
NP_001244894.1:p.Leu726Phe
|
|
NR_047563.2:n.2338G>T
|
|
|
NR_047564.2:n.2546G>T
|
|
|
NM_001257966.2:c.2128+5754G>T
|
NP_001244895.1:n.2128+5754G>T
|
|