ENST00000320005.6:c.2176_2177insCT
MANE Select
|
ENSP00000316605.5:p.Lys726ThrfsTer?
|
|
ENST00000681546.1:n.1996_1997insCT
|
|
|
ENST00000681746.1:c.*587_*588insCT
|
ENSP00000505959.1:n.*587_*588insCT
|
|
ENST00000320005.5:c.2176_2177insCT
|
ENSP00000316605.5:p.Lys726ThrfsTer?
|
|
ENST00000517327.5:c.276+2631_276+2632insCT
|
ENSP00000428329.1:n.276+2631_276+2632insCT
|
|
NM_019098.4:c.2176_2177insCT
|
NP_061971.3:p.Lys726ThrfsTer?
|
|
XM_011517138.1:c.1762_1763insCT
|
XP_011515440.1:p.Lys588ThrfsTer?
|
|
XM_011517138.2:c.1762_1763insCT
|
XP_011515440.1:p.Lys588ThrfsTer?
|
|
NM_019098.5:c.2176_2177insCT
MANE Select
|
NP_061971.3:p.Lys726ThrfsTer?
|
|