ENST00000367268.5:c.1198G=
MANE Select
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ENSP00000356237.4:p.Ala400=
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|
ENST00000367267.5:c.1198G=
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ENSP00000356236.1:p.Ala400=
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|
ENST00000367268.4:c.1198G=
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ENSP00000356237.4:p.Ala400=
|
|
NM_001136504.1:c.1198G=
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NP_001129976.1:p.Ala400=
|
|
NM_177402.4:c.1198G=
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NP_796376.2:p.Ala400=
|
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XM_011509192.1:c.1207G=
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XP_011507494.1:p.Ala403=
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XM_011509192.2:c.1207G=
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XP_011507494.1:p.Ala403=
|
|
XM_017000309.2:c.1378G=
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XP_016855798.1:p.Ala460=
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XM_017000310.2:c.1369G=
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XP_016855799.1:p.Ala457=
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XM_017000311.2:c.1207G=
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XP_016855800.1:p.Ala403=
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XM_017000312.1:c.1207G=
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XP_016855801.1:p.Ala403=
|
|
XM_017000313.1:c.1198G=
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XP_016855802.1:p.Ala400=
|
|
NM_177402.5:c.1198G=
MANE Select
|
NP_796376.2:p.Ala400=
|
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