ENST00000225964.10:c.3206C=
MANE Select
|
ENSP00000225964.6:p.Thr1069=
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|
ENST00000225964.9:c.3206C=
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ENSP00000225964.5:p.Thr1069=
|
|
ENST00000486572.1:n.24C=
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|
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ENST00000511732.1:n.150C=
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|
|
NM_000088.3:c.3206C= , LRG_1t1:c.3206C=
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NP_000079.2:p.Thr1069=
|
|
XM_005257058.3:c.2936C=
|
XP_005257115.2:p.Thr979=
|
|
XM_005257059.3:c.2288C=
|
XP_005257116.2:p.Thr763=
|
|
XM_011524341.1:c.3008C=
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XP_011522643.1:p.Thr1003=
|
|
XM_005257058.4:c.2936C=
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XP_005257115.2:p.Thr979=
|
|
XM_005257059.4:c.2288C=
|
XP_005257116.2:p.Thr763=
|
|
NM_000088.4:c.3206C=
MANE Select
|
NP_000079.2:p.Thr1069=
|
|