ENST00000299084.9:c.1185T=
MANE Select
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ENSP00000299084.4:p.Thr395=
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|
ENST00000299084.8:c.1185T=
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ENSP00000299084.4:p.Thr395=
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|
NM_152594.2:c.1185T=
|
NP_689807.1:p.Thr395=
|
|
XM_005254202.2:c.1221T=
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XP_005254259.1:p.Thr407=
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|
XM_005254203.3:c.963T=
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XP_005254260.1:p.Thr321=
|
|
XM_011521288.1:c.1122T=
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XP_011519590.1:p.Thr374=
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|
XM_011521289.1:c.1122T=
|
XP_011519591.1:p.Thr374=
|
|
XM_011521290.1:c.1122T=
|
XP_011519592.1:p.Thr374=
|
|
XM_005254202.3:c.1221T=
|
XP_005254259.1:p.Thr407=
|
|
XM_011521289.3:c.1122T=
|
XP_011519591.1:p.Thr374=
|
|
NM_152594.3:c.1185T=
MANE Select
|
NP_689807.1:p.Thr395=
|
|