ENST00000341947.7:c.3167T=
MANE Select
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ENSP00000339915.2:p.Ile1056=
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ENST00000341947.6:c.3167T=
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ENSP00000339915.2:p.Ile1056=
|
|
ENST00000361917.5:c.2846T=
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ENSP00000355123.1:p.Ile949=
|
|
ENST00000374708.8:c.2909T=
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ENSP00000363840.4:p.Ile970=
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|
ENST00000477772.1:n.272+5451T=
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|
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NM_080679.2:c.2846T=
|
NP_542410.2:p.Ile949=
|
|
NM_080680.2:c.3167T=
|
NP_542411.2:p.Ile1056=
|
|
NM_080681.2:c.2909T=
|
NP_542412.2:p.Ile970=
|
|
XM_011514298.1:c.2321T=
|
XP_011512600.1:p.Ile774=
|
|
XM_011514299.1:c.2453T=
|
XP_011512601.1:p.Ile818=
|
|
XM_011514300.1:c.2273T=
|
XP_011512602.1:p.Ile758=
|
|
XM_011514301.1:c.2210T=
|
XP_011512603.1:p.Ile737=
|
|
XM_011514302.1:c.2054T=
|
XP_011512604.1:p.Ile685=
|
|
XM_011514299.2:c.2453T=
|
XP_011512601.1:p.Ile818=
|
|
XM_011514300.2:c.2273T=
|
XP_011512602.1:p.Ile758=
|
|
XM_011514302.2:c.2054T=
|
XP_011512604.1:p.Ile685=
|
|
XM_017010250.1:c.3167T=
|
XP_016865739.1:p.Ile1056=
|
|
XM_017010251.2:c.1985T=
|
XP_016865740.1:p.Ile662=
|
|
NM_080680.3:c.3167T=
MANE Select
|
NP_542411.2:p.Ile1056=
|
|
NM_080681.3:c.2909T=
|
NP_542412.2:p.Ile970=
|
|
NM_080679.3:c.2846T=
|
NP_542410.2:p.Ile949=
|
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