ENST00000303941.4:c.2037A=
MANE Select
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ENSP00000306678.3:p.Leu679=
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|
ENST00000303941.3:c.2037A=
|
ENSP00000306678.3:p.Leu679=
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|
NM_178510.1:c.2037A=
|
NP_848605.1:p.Leu679=
|
|
XM_011542736.1:c.2070A=
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XP_011541038.1:p.Leu690=
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XM_011542737.1:c.2040A=
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XP_011541039.1:p.Leu680=
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XM_011542738.1:c.1848A=
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XP_011541040.1:p.Leu616=
|
|
XM_011542736.2:c.2070A=
|
XP_011541038.1:p.Leu690=
|
|
XM_011542737.2:c.2040A=
|
XP_011541039.1:p.Leu680=
|
|
XM_011542738.2:c.1848A=
|
XP_011541040.1:p.Leu616=
|
|
XM_017017475.1:c.2067A=
|
XP_016872964.1:p.Leu689=
|
|
NM_178510.2:c.2037A=
MANE Select
|
NP_848605.1:p.Leu679=
|
|