ENST00000373631.8:c.3798T>A
MANE Select
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ENSP00000362734.3:p.Ala1266=
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ENST00000373631.7:c.3798T>A
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ENSP00000362734.3:p.Ala1266=
|
|
ENST00000460253.1:c.2802T>A
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ENSP00000435279.1:p.Ala934=
|
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NM_173689.6:c.3798T>A
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NP_775960.4:p.Ala1266=
|
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NR_104603.1:n.2912T>A
|
|
|
XM_005251934.1:c.2802T>A
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XP_005251991.1:p.Ala934=
|
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XM_011518556.1:c.3771T>A
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XP_011516858.1:p.Ala1257=
|
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XM_011518557.1:c.3603T>A
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XP_011516859.1:p.Ala1201=
|
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XM_011518558.1:c.3603T>A
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XP_011516860.1:p.Ala1201=
|
|
XM_005251934.3:c.2802T>A
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XP_005251991.1:p.Ala934=
|
|
XM_011518556.3:c.3771T>A
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XP_011516858.1:p.Ala1257=
|
|
XM_011518557.3:c.3603T>A
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XP_011516859.1:p.Ala1201=
|
|
XM_011518558.3:c.3603T>A
|
XP_011516860.1:p.Ala1201=
|
|
NM_173689.7:c.3798T>A
MANE Select
|
NP_775960.4:p.Ala1266=
|
|
NR_104603.2:n.2912T>A
|
|
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