ENST00000373631.8:c.3800G>C
MANE Select
|
ENSP00000362734.3:p.Gly1267Ala
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|
ENST00000373631.7:c.3800G>C
|
ENSP00000362734.3:p.Gly1267Ala
|
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ENST00000460253.1:c.2804G>C
|
ENSP00000435279.1:p.Gly935Ala
|
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NM_173689.6:c.3800G>C
|
NP_775960.4:p.Gly1267Ala
|
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NR_104603.1:n.2914G>C
|
|
|
XM_005251934.1:c.2804G>C
|
XP_005251991.1:p.Gly935Ala
|
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XM_011518556.1:c.3773G>C
|
XP_011516858.1:p.Gly1258Ala
|
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XM_011518557.1:c.3605G>C
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XP_011516859.1:p.Gly1202Ala
|
|
XM_011518558.1:c.3605G>C
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XP_011516860.1:p.Gly1202Ala
|
|
XM_005251934.3:c.2804G>C
|
XP_005251991.1:p.Gly935Ala
|
|
XM_011518556.3:c.3773G>C
|
XP_011516858.1:p.Gly1258Ala
|
|
XM_011518557.3:c.3605G>C
|
XP_011516859.1:p.Gly1202Ala
|
|
XM_011518558.3:c.3605G>C
|
XP_011516860.1:p.Gly1202Ala
|
|
NM_173689.7:c.3800G>C
MANE Select
|
NP_775960.4:p.Gly1267Ala
|
|
NR_104603.2:n.2914G>C
|
|
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