ENST00000617695.5:c.7124C>G
|
ENSP00000481744.2:p.Ala2375Gly
|
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ENST00000618192.5:c.7388C>G
|
ENSP00000480802.2:p.Ala2463Gly
|
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ENST00000684985.1:n.755C>G
|
|
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ENST00000688150.1:n.463C>G
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|
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ENST00000421865.3:c.7124C>G
MANE Select
|
ENSP00000400365.2:p.Ala2375Gly
|
|
ENST00000421865.2:c.7124C>G
|
ENSP00000400365.2:p.Ala2375Gly
|
|
ENST00000617695.4:c.7124C>G
|
ENSP00000481744.1:p.Ala2375Gly
|
|
ENST00000618192.4:c.7121C>G
|
ENSP00000480802.1:p.Ala2374Gly
|
|
NM_000426.3:c.7124C>G , LRG_409t1:c.7124C>G
|
NP_000417.2:p.Ala2375Gly
|
|
NM_001079823.1:c.7124C>G
|
NP_001073291.1:p.Ala2375Gly
|
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XM_005266981.2:c.7388C>G
|
XP_005267038.1:p.Ala2463Gly
|
|
XM_005266982.2:c.7388C>G
|
XP_005267039.1:p.Ala2463Gly
|
|
XM_011535820.1:c.7382C>G
|
XP_011534122.1:p.Ala2461Gly
|
|
XM_005266981.3:c.7388C>G
|
XP_005267038.1:p.Ala2463Gly
|
|
XM_005266982.3:c.7388C>G
|
XP_005267039.1:p.Ala2463Gly
|
|
XM_011535820.2:c.7382C>G
|
XP_011534122.1:p.Ala2461Gly
|
|
XM_017010851.2:c.7394C>G
|
XP_016866340.1:p.Ala2465Gly
|
|
XM_017010852.1:c.5519C>G
|
XP_016866341.1:p.Ala1840Gly
|
|
NM_000426.4:c.7124C>G
MANE Select
|
NP_000417.3:p.Ala2375Gly
|
|
NM_001079823.2:c.7124C>G
|
NP_001073291.2:p.Ala2375Gly
|
|