ENST00000356884.11:c.1755_1758delinsCCTA
MANE Select
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ENSP00000349351.6:p.Leu585=
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ENST00000356884.10:c.1755_1758delinsCCTA
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ENSP00000349351.6:p.Leu585=
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|
ENST00000375512.3:c.1755_1758delinsCCTA
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ENSP00000364662.3:p.Leu585=
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|
NM_001003800.1:c.1755_1758delinsCCTA
|
NP_001003800.1:p.Leu585=
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NM_015250.3:c.1755_1758delinsCCTA
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NP_056065.1:p.Leu585=
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|
XM_017014551.1:c.1836_1839delinsCCTA
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XP_016870040.1:p.Leu612=
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|
NM_001003800.2:c.1755_1758delinsCCTA
MANE Select
|
NP_001003800.1:p.Leu585=
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|
NM_015250.4:c.1755_1758delinsCCTA
|
NP_056065.1:p.Leu585=
|
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