ENST00000399503.4:c.3167_3168insT
MANE Select
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ENSP00000382423.3:p.Ile1057HisfsTer8
|
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ENST00000399503.3:c.3167_3168insT
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ENSP00000382423.3:p.Ile1057HisfsTer8
|
|
NM_005921.1:c.3167_3168insT
|
NP_005912.1:p.Ile1057HisfsTer8
|
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XM_005248519.3:c.2789_2790insT
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XP_005248576.2:p.Ile931HisfsTer8
|
|
XM_011543406.1:c.2912_2913insT
|
XP_011541708.1:p.Ile972HisfsTer8
|
|
XM_011543407.1:c.2888_2889insT
|
XP_011541709.1:p.Ile964HisfsTer8
|
|
XM_011543408.1:c.3167_3168insT
|
XP_011541710.1:p.Ile1057HisfsTer8
|
|
XM_017009484.1:c.2756_2757insT
|
XP_016864973.1:p.Ile920HisfsTer8
|
|
XM_017009485.1:c.2678_2679insT
|
XP_016864974.1:p.Ile894HisfsTer8
|
|
XR_001742068.2:n.3198_3199insT
|
|
|
NM_005921.2:c.3167_3168insT
MANE Select
|
NP_005912.1:p.Ile1057HisfsTer8
|
|