ENST00000261024.7:c.135G>C
MANE Select
|
ENSP00000261024.3:p.Ala45=
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ENST00000261024.6:c.135G>C
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ENSP00000261024.2:p.Ala45=
|
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ENST00000418714.1:n.576G>C
|
|
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ENST00000427241.5:c.135G>C
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ENSP00000390005.1:p.Ala45=
|
|
ENST00000455320.5:c.135G>C
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ENSP00000413549.1:p.Ala45=
|
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ENST00000479598.5:n.416G>C
|
|
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NM_014585.5:c.135G>C , LRG_837t1:c.135G>C
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NP_055400.1:p.Ala45=
|
|
XM_005246505.1:c.15G>C
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XP_005246562.1:p.Ala5=
|
|
XM_005246505.2:c.15G>C
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XP_005246562.1:p.Ala5=
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XM_017003938.2:c.15G>C
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XP_016859427.1:p.Ala5=
|
|
NM_014585.6:c.135G>C
MANE Select
|
NP_055400.1:p.Ala45=
|
|