ENST00000392793.6:c.5097C>G
(TECTA)
MANE Select
|
ENSP00000376543.1:p.Gly1699=
|
|
ENST00000642222.1:c.5082C>G
(TECTA)
|
ENSP00000493855.1:p.Gly1694=
|
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ENST00000645008.1:c.2389C>G
(TECTA)
|
|
|
ENST00000646278.1:n.1018C>G
(TECTA)
|
|
|
ENST00000264037.2:c.5097C>G
(TECTA)
|
ENSP00000264037.2:p.Gly1699=
|
|
ENST00000392793.5:c.5097C>G
(TECTA)
|
ENSP00000376543.1:p.Gly1699=
|
|
NM_005422.2:c.5097C>G
(TECTA)
|
NP_005413.2:p.Gly1699=
|
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NM_001378761.1:c.6039C>G
(TBCEL-TECTA)
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NP_001365690.1:p.Gly2013=
|
|
NM_005422.4:c.5097C>G
(TECTA)
MANE Select
|
NP_005413.2:p.Gly1699=
|
|