ENST00000295754.10:c.1613T=
MANE Select
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ENSP00000295754.5:p.Phe538=
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ENST00000672050.1:n.497T=
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|
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ENST00000672866.1:n.3209T=
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|
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ENST00000673203.1:n.491T=
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|
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ENST00000295754.9:c.1613T=
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ENSP00000295754.5:p.Phe538=
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|
ENST00000359013.4:c.1688T=
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ENSP00000351905.4:p.Phe563=
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NM_001024847.2:c.1688T= , LRG_779t1:c.1688T=
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NP_001020018.1:p.Phe563=
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|
NM_003242.5:c.1613T=
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NP_003233.4:p.Phe538=
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XM_011534043.1:c.1640T=
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XP_011532345.1:p.Phe547=
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XM_011534044.1:c.1565T=
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XP_011532346.1:p.Phe522=
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XM_011534045.1:c.1508T=
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XP_011532347.1:p.Phe503=
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|
XM_011534043.2:c.1640T=
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XP_011532345.1:p.Phe547=
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|
XM_011534045.3:c.1508T=
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XP_011532347.1:p.Phe503=
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|
XM_017007106.1:c.1508T=
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XP_016862595.1:p.Phe503=
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|
NM_003242.6:c.1613T=
MANE Select
|
NP_003233.4:p.Phe538=
|
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