ENST00000696142.1:c.*249dup
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ENSP00000512434.1:n.*249dup
|
|
ENST00000696143.1:c.708dup
|
ENSP00000512435.1:n.708dup
|
|
ENST00000696153.1:c.683dup
|
ENSP00000512444.1:p.His228GlnfsTer?
|
|
ENST00000256474.3:c.572dup
MANE Select
|
ENSP00000256474.3:p.His191GlnfsTer?
|
|
ENST00000256474.2:c.572dup
|
ENSP00000256474.2:p.His191GlnfsTer?
|
|
ENST00000345392.2:c.449dup
|
ENSP00000344757.2:p.His150GlnfsTer?
|
|
ENST00000477538.1:n.708dup
|
|
|
NM_000551.3:c.572dup , LRG_322t1:c.572dup
|
NP_000542.1:p.His191GlnfsTer?
|
|
NM_198156.2:c.449dup
|
NP_937799.1:p.His150GlnfsTer?
|
|
NM_001354723.1:c.*126dup
|
NP_001341652.1:n.*126dup
|
|
NM_000551.4:c.572dup
MANE Select
|
NP_000542.1:p.His191GlnfsTer?
|
|
NM_001354723.2:c.*126dup
|
NP_001341652.1:n.*126dup
|
|
NM_198156.3:c.449dup
|
NP_937799.1:p.His150GlnfsTer?
|
|