ENST00000367400.8:c.4008G>C
MANE Select
|
ENSP00000356370.3:p.Leu1336Phe
|
|
ENST00000367399.6:c.3672G>C
|
ENSP00000356369.2:p.Leu1224Phe
|
|
ENST00000367400.7:c.4008G>C
|
ENSP00000356370.3:p.Leu1336Phe
|
|
ENST00000448952.1:c.242G>C
|
ENSP00000395407.1:n.242G>C
|
|
ENST00000484075.5:c.*119G>C
|
ENSP00000433932.1:n.*119G>C
|
|
ENST00000535699.5:c.3936G>C
|
ENSP00000438786.1:p.Leu1312Phe
|
|
ENST00000538660.5:c.2400G>C
|
ENSP00000438091.1:p.Leu800Phe
|
|
NM_001193640.1:c.3672G>C
|
NP_001180569.1:p.Leu1224Phe
|
|
NM_001257965.1:c.3936G>C
|
NP_001244894.1:p.Leu1312Phe
|
|
NM_001257966.1:c.2400G>C
|
NP_001244895.1:p.Leu800Phe
|
|
NM_201253.2:c.4008G>C
|
NP_957705.1:p.Leu1336Phe
|
|
NR_047563.1:n.4009G>C
|
|
|
NR_047564.1:n.4459G>C
|
|
|
XM_011509366.1:c.*113G>C
|
XP_011507668.1:n.*113G>C
|
|
XM_011509367.1:c.3881G>C
|
XP_011507669.1:p.Trp1294Ser
|
|
XM_011509368.1:c.3426G>C
|
XP_011507670.1:p.Leu1142Phe
|
|
XM_011509369.1:c.2451G>C
|
XP_011507671.1:p.Leu817Phe
|
|
XM_011509369.2:c.2451G>C
|
XP_011507671.1:p.Leu817Phe
|
|
XM_017000851.1:c.3165G>C
|
XP_016856340.1:p.Leu1055Phe
|
|
XM_017000852.1:c.4143G>C
|
XP_016856341.1:p.Leu1381Phe
|
|
NM_201253.3:c.4008G>C
MANE Select
|
NP_957705.1:p.Leu1336Phe
|
|
NM_001193640.2:c.3672G>C
|
NP_001180569.1:p.Leu1224Phe
|
|
NM_001257965.2:c.3936G>C
|
NP_001244894.1:p.Leu1312Phe
|
|
NR_047563.2:n.3961G>C
|
|
|
NR_047564.2:n.4411G>C
|
|
|
NM_001257966.2:c.2400G>C
|
NP_001244895.1:p.Leu800Phe
|
|