ENST00000241453.12:c.2432A>G
MANE Select
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ENSP00000241453.7:p.Asp811Gly
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ENST00000241453.11:c.2432A>G
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ENSP00000241453.7:p.Asp811Gly
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ENST00000380987.2:c.*344A>G
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ENSP00000370374.2:n.*344A>G
|
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NM_004119.2:c.2432A>G , LRG_457t1:c.2432A>G
|
NP_004110.2:p.Asp811Gly
|
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NR_130706.1:n.2646A>G
|
|
|
XM_011535015.1:c.2375A>G
|
XP_011533317.1:p.Asp792Gly
|
|
XM_011535016.1:c.1907A>G
|
XP_011533318.1:p.Asp636Gly
|
|
XM_011535017.1:c.1907A>G
|
XP_011533319.1:p.Asp636Gly
|
|
XM_011535018.1:c.1907A>G
|
XP_011533320.1:p.Asp636Gly
|
|
XM_011535015.2:c.2375A>G
|
XP_011533317.1:p.Asp792Gly
|
|
XM_011535017.2:c.1907A>G
|
XP_011533319.1:p.Asp636Gly
|
|
XM_011535018.2:c.1907A>G
|
XP_011533320.1:p.Asp636Gly
|
|
XM_017020486.1:c.2216A>G
|
XP_016875975.1:p.Asp739Gly
|
|
XM_017020487.1:c.1907A>G
|
XP_016875976.1:p.Asp636Gly
|
|
XM_017020488.1:c.1553A>G
|
XP_016875977.1:p.Asp518Gly
|
|
XM_017020489.1:c.1535A>G
|
XP_016875978.1:p.Asp512Gly
|
|
NM_004119.3:c.2432A>G
MANE Select
|
NP_004110.2:p.Asp811Gly
|
|
NR_130706.2:n.2630A>G
|
|
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