ENST00000336112.9:c.4183A>G
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ENSP00000337250.5:p.Thr1395Ala
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ENST00000435504.9:c.4186A>G
MANE Select
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ENSP00000391447.3:p.Thr1396Ala
|
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ENST00000336112.8:c.4102A>G
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ENSP00000337250.4:p.Thr1368Ala
|
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ENST00000404843.5:c.2635A>G
|
ENSP00000383920.1:p.Thr879Ala
|
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ENST00000435504.8:c.4186A>G
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ENSP00000391447.3:p.Thr1396Ala
|
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NM_018263.4:c.4186A>G
|
NP_060733.4:p.Thr1396Ala
|
|
XM_006712039.2:c.3820A>G
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XP_006712102.1:p.Thr1274Ala
|
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XM_006712040.1:c.3406A>G
|
XP_006712103.1:p.Thr1136Ala
|
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XM_011532950.1:c.4183A>G
|
XP_011531252.1:p.Thr1395Ala
|
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XM_011532951.1:c.4012A>G
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XP_011531253.1:p.Thr1338Ala
|
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NM_018263.5:c.4186A>G
|
NP_060733.4:p.Thr1396Ala
|
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XM_006712039.3:c.3820A>G
|
XP_006712102.1:p.Thr1274Ala
|
|
XM_006712040.2:c.3406A>G
|
XP_006712103.1:p.Thr1136Ala
|
|
XM_011532950.3:c.4183A>G
|
XP_011531252.1:p.Thr1395Ala
|
|
XM_011532951.2:c.4012A>G
|
XP_011531253.1:p.Thr1338Ala
|
|
XM_017004430.1:c.3406A>G
|
XP_016859919.1:p.Thr1136Ala
|
|
XM_024452974.1:c.4366A>G
|
XP_024308742.1:p.Thr1456Ala
|
|
NM_001369346.1:c.4012A>G
|
NP_001356275.1:p.Thr1338Ala
|
|
NM_001369347.1:c.3406A>G
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NP_001356276.1:p.Thr1136Ala
|
|
NM_018263.6:c.4186A>G
MANE Select
|
NP_060733.4:p.Thr1396Ala
|
|