ENST00000367400.8:c.4201G>C
MANE Select
|
ENSP00000356370.3:p.Ala1401Pro
|
|
ENST00000367399.6:c.3865G>C
|
ENSP00000356369.2:p.Ala1289Pro
|
|
ENST00000367400.7:c.4201G>C
|
ENSP00000356370.3:p.Ala1401Pro
|
|
ENST00000448952.1:c.435G>C
|
ENSP00000395407.1:n.435G>C
|
|
ENST00000484075.5:c.*312G>C
|
ENSP00000433932.1:n.*312G>C
|
|
ENST00000535699.5:c.4129G>C
|
ENSP00000438786.1:p.Ala1377Pro
|
|
ENST00000538660.5:c.2593G>C
|
ENSP00000438091.1:p.Ala865Pro
|
|
NM_001193640.1:c.3865G>C
|
NP_001180569.1:p.Ala1289Pro
|
|
NM_001257965.1:c.4129G>C
|
NP_001244894.1:p.Ala1377Pro
|
|
NM_001257966.1:c.2593G>C
|
NP_001244895.1:p.Ala865Pro
|
|
NM_201253.2:c.4201G>C
|
NP_957705.1:p.Ala1401Pro
|
|
NR_047563.1:n.4202G>C
|
|
|
NR_047564.1:n.4652G>C
|
|
|
XM_011509366.1:c.*306G>C
|
XP_011507668.1:n.*306G>C
|
|
XM_011509367.1:c.*180G>C
|
XP_011507669.1:n.*180G>C
|
|
XM_011509368.1:c.3619G>C
|
XP_011507670.1:p.Ala1207Pro
|
|
XM_011509369.1:c.2644G>C
|
XP_011507671.1:p.Ala882Pro
|
|
XM_011509369.2:c.2644G>C
|
XP_011507671.1:p.Ala882Pro
|
|
XM_017000851.1:c.3358G>C
|
XP_016856340.1:p.Ala1120Pro
|
|
XM_017000852.1:c.4336G>C
|
XP_016856341.1:p.Ala1446Pro
|
|
NM_201253.3:c.4201G>C
MANE Select
|
NP_957705.1:p.Ala1401Pro
|
|
NM_001193640.2:c.3865G>C
|
NP_001180569.1:p.Ala1289Pro
|
|
NM_001257965.2:c.4129G>C
|
NP_001244894.1:p.Ala1377Pro
|
|
NR_047563.2:n.4154G>C
|
|
|
NR_047564.2:n.4604G>C
|
|
|
NM_001257966.2:c.2593G>C
|
NP_001244895.1:p.Ala865Pro
|
|