ENST00000380707.9:c.733C>G
MANE Select
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ENSP00000370083.4:p.Pro245Ala
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ENST00000351205.8:c.733C>G
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ENSP00000305857.5:p.Pro245Ala
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ENST00000380707.8:c.733C>G
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ENSP00000370083.4:p.Pro245Ala
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ENST00000503079.6:c.637C>G
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ENSP00000428128.1:p.Pro213Ala
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ENST00000506163.5:c.733C>G
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ENSP00000424926.1:p.Pro245Ala
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ENST00000506239.6:c.733C>G
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ENSP00000422679.2:p.Pro245Ala
|
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ENST00000507905.6:c.427C>G
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ENSP00000430657.1:n.427C>G
|
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ENST00000513228.1:n.300C>G
|
|
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ENST00000514951.5:c.532C>G
|
ENSP00000423298.1:p.Pro178Ala
|
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ENST00000518504.5:n.250C>G
|
|
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ENST00000625245.2:c.733C>G
|
ENSP00000486539.1:p.Pro245Ala
|
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NM_000344.3:c.733C>G , LRG_676t1:c.733C>G
|
NP_000335.1:p.Pro245Ala
|
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NM_001297715.1:c.733C>G
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NP_001284644.1:p.Pro245Ala
|
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NM_022874.2:c.637C>G
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NP_075012.1:p.Pro213Ala
|
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XM_011543596.1:c.733C>G
|
XP_011541898.1:p.Pro245Ala
|
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XM_011543597.1:c.532C>G
|
XP_011541899.1:p.Pro178Ala
|
|
XM_011543598.1:c.436C>G
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XP_011541900.1:p.Pro146Ala
|
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XM_011543598.3:c.436C>G
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XP_011541900.1:p.Pro146Ala
|
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XM_017009786.1:c.637C>G
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XP_016865275.1:p.Pro213Ala
|
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NM_000344.4:c.733C>G
MANE Select
|
NP_000335.1:p.Pro245Ala
|
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