ENST00000222214.10:c.342C=
MANE Select
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ENSP00000222214.4:p.Gly114=
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ENST00000222214.9:c.342C=
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ENSP00000222214.4:p.Gly114=
|
|
ENST00000421816.6:n.320C=
|
|
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ENST00000585420.5:n.707C=
|
|
|
ENST00000587072.1:c.390C=
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ENSP00000468584.1:p.Gly130=
|
|
ENST00000587832.5:n.399C=
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|
|
ENST00000588905.5:c.306C=
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ENSP00000465770.1:p.Gly102=
|
|
ENST00000589039.5:c.279C=
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ENSP00000465618.1:p.Gly93=
|
|
ENST00000590530.5:c.397C=
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ENSP00000468452.1:p.Leu133=
|
|
ENST00000590627.5:n.707C=
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|
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ENST00000591043.1:n.378C=
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|
|
ENST00000591470.5:c.342C=
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ENSP00000466845.1:p.Gly114=
|
|
NM_000159.3:c.342C=
|
NP_000150.1:p.Gly114=
|
|
NM_013976.3:c.342C=
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NP_039663.1:p.Gly114=
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|
NR_102316.1:n.505C=
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|
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NR_102317.1:n.758C=
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|
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XM_006722721.2:c.342C=
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XP_006722784.1:p.Gly114=
|
|
XM_011527899.1:c.342C=
|
XP_011526201.1:p.Gly114=
|
|
XM_011527900.1:c.342C=
|
XP_011526202.1:p.Gly114=
|
|
XM_011527899.2:c.342C=
|
XP_011526201.1:p.Gly114=
|
|
XM_011527900.2:c.342C=
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XP_011526202.1:p.Gly114=
|
|
XM_017026580.1:c.342C=
|
XP_016882069.1:p.Gly114=
|
|
NM_000159.4:c.342C=
MANE Select
|
NP_000150.1:p.Gly114=
|
|
NM_013976.4:c.342C=
|
NP_039663.1:p.Gly114=
|
|
NM_013976.5:c.342C=
|
NP_039663.1:p.Gly114=
|
|