ENST00000258439.8:c.435C>G
MANE Select
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ENSP00000258439.3:p.Gly145=
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ENST00000258439.7:c.435C>G
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ENSP00000258439.2:p.Gly145=
|
|
ENST00000432959.1:c.435C>G
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ENSP00000416660.1:p.Gly145=
|
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ENST00000435268.1:c.183C>G
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ENSP00000411810.1:p.Gly61=
|
|
NM_001193304.2:c.435C>G
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NP_001180233.1:p.Gly145=
|
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NM_017849.3:c.435C>G , LRG_528t1:c.435C>G
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NP_060319.1:p.Gly145=
|
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XM_017004450.1:c.-484C>G
|
XP_016859939.1:n.-484C>G
|
|
XM_017004452.1:c.183C>G
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XP_016859941.1:p.Gly61=
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NM_001193304.3:c.435C>G
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NP_001180233.1:p.Gly145=
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NM_017849.4:c.435C>G
MANE Select
|
NP_060319.1:p.Gly145=
|
|