ENST00000455140.7:c.2587-1114G>T
MANE Select
|
ENSP00000393313.1:n.2587-1114G>T
|
|
ENST00000455140.6:c.2587-1114G>T
|
ENSP00000393313.1:n.2587-1114G>T
|
|
ENST00000594851.5:c.69-1114G>T
|
|
|
ENST00000602022.5:c.*189-1114G>T
|
ENSP00000471981.1:n.*189-1114G>T
|
|
NM_001258374.1:c.2587-1114G>T
|
NP_001245303.1:n.2587-1114G>T
|
|
NR_047665.1:n.2521-1114G>T
|
|
|
XM_017027086.2:c.2635-1114G>T
|
XP_016882575.1:n.2635-1114G>T
|
|
XM_017027087.2:c.2695G>T
|
XP_016882576.1:p.Glu899Ter
|
|
XM_017027088.2:c.2588G>T
|
XP_016882577.1:p.Arg863Ile
|
|
XM_017027089.2:c.2528-1114G>T
|
XP_016882578.1:n.2528-1114G>T
|
|
XM_017027090.2:c.2248-1114G>T
|
XP_016882579.1:n.2248-1114G>T
|
|
XM_017027091.2:c.2381-1114G>T
|
XP_016882580.1:n.2381-1114G>T
|
|
NM_001258374.2:c.2587-1114G>T
|
NP_001245303.1:n.2587-1114G>T
|
|
NM_001258374.3:c.2587-1114G>T
MANE Select
|
NP_001245303.1:n.2587-1114G>T
|
|
NR_047665.2:n.2479-1114G>T
|
|
|