ENST00000367400.8:c.4205T>A
MANE Select
|
ENSP00000356370.3:p.Met1402Lys
|
|
ENST00000367399.6:c.3869T>A
|
ENSP00000356369.2:p.Met1290Lys
|
|
ENST00000367400.7:c.4205T>A
|
ENSP00000356370.3:p.Met1402Lys
|
|
ENST00000448952.1:c.439T>A
|
ENSP00000395407.1:n.439T>A
|
|
ENST00000484075.5:c.*316T>A
|
ENSP00000433932.1:n.*316T>A
|
|
ENST00000535699.5:c.4133T>A
|
ENSP00000438786.1:p.Met1378Lys
|
|
ENST00000538660.5:c.2597T>A
|
ENSP00000438091.1:p.Met866Lys
|
|
NM_001193640.1:c.3869T>A
|
NP_001180569.1:p.Met1290Lys
|
|
NM_001257965.1:c.4133T>A
|
NP_001244894.1:p.Met1378Lys
|
|
NM_001257966.1:c.2597T>A
|
NP_001244895.1:p.Met866Lys
|
|
NM_201253.2:c.4205T>A
|
NP_957705.1:p.Met1402Lys
|
|
NR_047563.1:n.4206T>A
|
|
|
NR_047564.1:n.4656T>A
|
|
|
XM_011509366.1:c.*310T>A
|
XP_011507668.1:n.*310T>A
|
|
XM_011509367.1:c.*184T>A
|
XP_011507669.1:n.*184T>A
|
|
XM_011509368.1:c.3623T>A
|
XP_011507670.1:p.Met1208Lys
|
|
XM_011509369.1:c.2648T>A
|
XP_011507671.1:p.Met883Lys
|
|
XM_011509369.2:c.2648T>A
|
XP_011507671.1:p.Met883Lys
|
|
XM_017000851.1:c.3362T>A
|
XP_016856340.1:p.Met1121Lys
|
|
XM_017000852.1:c.4340T>A
|
XP_016856341.1:p.Met1447Lys
|
|
NM_201253.3:c.4205T>A
MANE Select
|
NP_957705.1:p.Met1402Lys
|
|
NM_001193640.2:c.3869T>A
|
NP_001180569.1:p.Met1290Lys
|
|
NM_001257965.2:c.4133T>A
|
NP_001244894.1:p.Met1378Lys
|
|
NR_047563.2:n.4158T>A
|
|
|
NR_047564.2:n.4608T>A
|
|
|
NM_001257966.2:c.2597T>A
|
NP_001244895.1:p.Met866Lys
|
|