ENST00000617695.5:c.7691G>C
|
ENSP00000481744.2:p.Gly2564Ala
|
|
ENST00000618192.5:c.7967G>C
|
ENSP00000480802.2:p.Gly2656Ala
|
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ENST00000421865.3:c.7703G>C
MANE Select
|
ENSP00000400365.2:p.Gly2568Ala
|
|
ENST00000421865.2:c.7703G>C
|
ENSP00000400365.2:p.Gly2568Ala
|
|
ENST00000617695.4:c.7691G>C
|
ENSP00000481744.1:p.Gly2564Ala
|
|
ENST00000618192.4:c.7700G>C
|
ENSP00000480802.1:p.Gly2567Ala
|
|
NM_000426.3:c.7703G>C , LRG_409t1:c.7703G>C
|
NP_000417.2:p.Gly2568Ala
|
|
NM_001079823.1:c.7691G>C
|
NP_001073291.1:p.Gly2564Ala
|
|
XM_005266981.2:c.7967G>C
|
XP_005267038.1:p.Gly2656Ala
|
|
XM_005266982.2:c.7955G>C
|
XP_005267039.1:p.Gly2652Ala
|
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XM_011535820.1:c.7961G>C
|
XP_011534122.1:p.Gly2654Ala
|
|
XM_005266981.3:c.7967G>C
|
XP_005267038.1:p.Gly2656Ala
|
|
XM_005266982.3:c.7955G>C
|
XP_005267039.1:p.Gly2652Ala
|
|
XM_011535820.2:c.7961G>C
|
XP_011534122.1:p.Gly2654Ala
|
|
XM_017010851.2:c.7973G>C
|
XP_016866340.1:p.Gly2658Ala
|
|
XM_017010852.1:c.6098G>C
|
XP_016866341.1:p.Gly2033Ala
|
|
NM_000426.4:c.7703G>C
MANE Select
|
NP_000417.3:p.Gly2568Ala
|
|
NM_001079823.2:c.7691G>C
|
NP_001073291.2:p.Gly2564Ala
|
|