ENST00000376883.2:c.1452C>A
MANE Select
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ENSP00000366080.2:p.Gly484=
|
|
ENST00000488757.6:c.1236C>A
|
ENSP00000418259.2:p.Gly412=
|
|
ENST00000376881.4:c.1200C>A
|
ENSP00000366078.4:p.Gly400=
|
|
ENST00000376883.1:c.1392C>A
|
ENSP00000366080.1:p.Gly464=
|
|
ENST00000488757.5:c.1452C>A
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ENSP00000418259.1:p.Gly484=
|
|
NM_001109809.2:c.1452C>A
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NP_001103279.2:p.Gly484=
|
|
XM_006715087.2:c.1236C>A
|
XP_006715150.1:p.Gly412=
|
|
XM_011514570.1:c.1452C>A
|
XP_011512872.1:p.Gly484=
|
|
NM_001109809.3:c.1452C>A
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NP_001103279.2:p.Gly484=
|
|
NM_001366333.1:c.1236C>A
|
NP_001353262.1:p.Gly412=
|
|
NM_001109809.4:c.1452C>A
|
NP_001103279.2:p.Gly484=
|
|
NM_001366333.2:c.1236C>A
|
NP_001353262.1:p.Gly412=
|
|
NM_001109809.5:c.1452C>A
MANE Select
|
NP_001103279.2:p.Gly484=
|
|