ENST00000353578.9:c.6230G>C
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ENSP00000315873.4:p.Gly2077Ala
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ENST00000295550.9:c.6848G>C
MANE Select
|
ENSP00000295550.4:p.Gly2283Ala
|
|
ENST00000295550.8:c.6848G>C
|
ENSP00000295550.4:p.Gly2283Ala
|
|
ENST00000347401.7:c.5027G>C
|
ENSP00000315609.4:p.Gly1676Ala
|
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ENST00000353578.8:c.6230G>C
|
ENSP00000315873.4:p.Gly2077Ala
|
|
ENST00000409809.5:c.6230G>C
|
ENSP00000386844.1:p.Gly2077Ala
|
|
ENST00000472056.5:c.5027G>C
|
ENSP00000418285.1:p.Gly1676Ala
|
|
ENST00000491769.1:n.1102G>C
|
|
|
NM_004369.3:c.6848G>C , LRG_473t1:c.6848G>C
|
NP_004360.2:p.Gly2283Ala
|
|
NM_057166.4:c.5027G>C
|
NP_476507.3:p.Gly1676Ala
|
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NM_057167.3:c.6230G>C
|
NP_476508.2:p.Gly2077Ala
|
|
XM_005246065.1:c.6248G>C
|
XP_005246122.1:p.Gly2083Ala
|
|
XM_005246066.1:c.5627G>C
|
XP_005246123.1:p.Gly1876Ala
|
|
XM_006712253.1:c.6347G>C
|
XP_006712316.1:p.Gly2116Ala
|
|
XM_011510574.1:c.6845G>C
|
XP_011508876.1:p.Gly2282Ala
|
|
XM_011510575.1:c.4442G>C
|
XP_011508877.1:p.Gly1481Ala
|
|
XM_017003304.1:c.4442G>C
|
XP_016858793.1:p.Gly1481Ala
|
|
XM_024452684.1:c.5627G>C
|
XP_024308452.1:p.Gly1876Ala
|
|
NM_004369.4:c.6848G>C
MANE Select
|
NP_004360.2:p.Gly2283Ala
|
|
NM_057166.5:c.5027G>C
|
NP_476507.3:p.Gly1676Ala
|
|
NM_057167.4:c.6230G>C
|
NP_476508.2:p.Gly2077Ala
|
|