ENST00000254108.12:c.525T>A
MANE Select
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ENSP00000254108.8:p.Gly175=
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ENST00000254108.11:c.525T>A
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ENSP00000254108.7:p.Gly175=
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ENST00000380244.7:c.522T>A
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ENSP00000369594.3:p.Gly174=
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ENST00000487509.6:n.590T>A
|
|
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ENST00000566605.5:c.525T>A
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ENSP00000455073.1:p.Gly175=
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ENST00000568685.1:c.525T>A
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ENSP00000455282.1:p.Gly175=
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NM_001170634.1:c.522T>A
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NP_001164105.1:p.Gly174=
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NM_001170937.1:c.513T>A
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NP_001164408.1:p.Gly171=
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NM_004960.3:c.525T>A , LRG_655t1:c.525T>A
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NP_004951.1:p.Gly175=
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NR_028388.2:n.630T>A
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|
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XM_005255233.3:c.-56T>A
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XP_005255290.1:n.-56T>A
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XM_011545781.1:c.519T>A
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XP_011544083.1:p.Gly173=
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XM_011545782.1:c.-56T>A
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XP_011544084.1:n.-56T>A
|
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XM_005255233.5:c.-56T>A
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XP_005255290.1:n.-56T>A
|
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XM_011545782.2:c.-56T>A
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XP_011544084.1:n.-56T>A
|
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XM_024450221.1:c.516T>A
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XP_024305989.1:p.Gly172=
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NM_004960.4:c.525T>A
MANE Select
|
NP_004951.1:p.Gly175=
|
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