ENST00000367400.8:c.3316T>C
MANE Select
|
ENSP00000356370.3:p.Tyr1106His
|
|
ENST00000638467.1:c.3316T>C
|
ENSP00000491102.1:p.Tyr1106His
|
|
ENST00000681519.1:c.2197T>C
|
ENSP00000505267.1:p.Tyr733His
|
|
ENST00000367397.1:c.1459T>C
|
ENSP00000356367.1:p.Tyr487His
|
|
ENST00000367399.6:c.2980T>C
|
ENSP00000356369.2:p.Tyr994His
|
|
ENST00000367400.7:c.3316T>C
|
ENSP00000356370.3:p.Tyr1106His
|
|
ENST00000484075.5:c.3316T>C
|
ENSP00000433932.1:p.Tyr1106His
|
|
ENST00000535699.5:c.3244T>C
|
ENSP00000438786.1:p.Tyr1082His
|
|
ENST00000538660.5:c.2129-421T>C
|
ENSP00000438091.1:n.2129-421T>C
|
|
NM_001193640.1:c.2980T>C
|
NP_001180569.1:p.Tyr994His
|
|
NM_001257965.1:c.3244T>C
|
NP_001244894.1:p.Tyr1082His
|
|
NM_001257966.1:c.2129-421T>C
|
NP_001244895.1:n.2129-421T>C
|
|
NM_201253.2:c.3316T>C
|
NP_957705.1:p.Tyr1106His
|
|
NR_047563.1:n.3317T>C
|
|
|
NR_047564.1:n.3525T>C
|
|
|
XM_011509365.1:c.3316T>C
|
XP_011507667.1:p.Tyr1106His
|
|
XM_011509366.1:c.3316T>C
|
XP_011507668.1:p.Tyr1106His
|
|
XM_011509367.1:c.3316T>C
|
XP_011507669.1:p.Tyr1106His
|
|
XM_011509368.1:c.2734T>C
|
XP_011507670.1:p.Tyr912His
|
|
XM_011509369.1:c.1759T>C
|
XP_011507671.1:p.Tyr587His
|
|
XM_011509365.2:c.3316T>C
|
XP_011507667.1:p.Tyr1106His
|
|
XM_011509369.2:c.1759T>C
|
XP_011507671.1:p.Tyr587His
|
|
XM_017000851.1:c.2473T>C
|
XP_016856340.1:p.Tyr825His
|
|
XM_017000852.1:c.3451T>C
|
XP_016856341.1:p.Tyr1151His
|
|
NM_201253.3:c.3316T>C
MANE Select
|
NP_957705.1:p.Tyr1106His
|
|
NM_001193640.2:c.2980T>C
|
NP_001180569.1:p.Tyr994His
|
|
NM_001257965.2:c.3244T>C
|
NP_001244894.1:p.Tyr1082His
|
|
NR_047563.2:n.3269T>C
|
|
|
NR_047564.2:n.3477T>C
|
|
|
NM_001257966.2:c.2129-421T>C
|
NP_001244895.1:n.2129-421T>C
|
|