ENST00000696142.1:c.*62_*63insAGA
|
ENSP00000512434.1:n.*62_*63insAGA
|
|
ENST00000696143.1:c.600-3229_600-3228insAGA
|
ENSP00000512435.1:n.600-3229_600-3228insAGA
|
|
ENST00000696153.1:c.385_386insAGA
|
ENSP00000512444.1:p.Leu129delinsGlnMet
|
|
ENST00000256474.3:c.385_386insAGA
MANE Select
|
ENSP00000256474.3:p.Leu129delinsGlnMet
|
|
ENST00000256474.2:c.385_386insAGA
|
ENSP00000256474.2:p.Leu129delinsGlnMet
|
|
ENST00000345392.2:c.341-3229_341-3228insAGA
|
ENSP00000344757.2:n.341-3229_341-3228insAGA
|
|
ENST00000477538.1:n.521_522insAGA
|
|
|
NM_000551.3:c.385_386insAGA , LRG_322t1:c.385_386insAGA
|
NP_000542.1:p.Leu129delinsGlnMet
|
|
NM_198156.2:c.341-3229_341-3228insAGA
|
NP_937799.1:n.341-3229_341-3228insAGA
|
|
XM_011534078.1:c.*62_*63insAGA
|
XP_011532380.1:n.*62_*63insAGA
|
|
NM_001354723.1:c.*18-3229_*18-3228insAGA
|
NP_001341652.1:n.*18-3229_*18-3228insAGA
|
|
NM_000551.4:c.385_386insAGA
MANE Select
|
NP_000542.1:p.Leu129delinsGlnMet
|
|
NM_001354723.2:c.*18-3229_*18-3228insAGA
|
NP_001341652.1:n.*18-3229_*18-3228insAGA
|
|
NM_198156.3:c.341-3229_341-3228insAGA
|
NP_937799.1:n.341-3229_341-3228insAGA
|
|