ENST00000320005.6:c.2181_2185delinsAAAAG
MANE Select
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ENSP00000316605.5:p.Gln727=
|
|
ENST00000681546.1:n.2001_2005delinsAAAAG
|
|
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ENST00000681746.1:c.*592_*596delinsAAAAG
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ENSP00000505959.1:n.*592_*596delinsAAAAG
|
|
ENST00000320005.5:c.2181_2185delinsAAAAG
|
ENSP00000316605.5:p.Gln727=
|
|
ENST00000517327.5:c.276+2636_276+2640delinsAAAAG
|
ENSP00000428329.1:n.276+2636_276+2640delinsAAAAG
|
|
NM_019098.4:c.2181_2185delinsAAAAG
|
NP_061971.3:p.Gln727=
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|
XM_011517138.1:c.1767_1771delinsAAAAG
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XP_011515440.1:p.Gln589=
|
|
XM_011517138.2:c.1767_1771delinsAAAAG
|
XP_011515440.1:p.Gln589=
|
|
NM_019098.5:c.2181_2185delinsAAAAG
MANE Select
|
NP_061971.3:p.Gln727=
|
|