ENST00000395348.8:c.773C>A
MANE Select
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ENSP00000378757.3:p.Thr258Lys
|
|
ENST00000395347.1:c.773C>A
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ENSP00000378756.1:p.Thr258Lys
|
|
ENST00000395348.7:c.773C>A
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ENSP00000378757.3:p.Thr258Lys
|
|
NM_194298.2:c.773C>A
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NP_919274.1:p.Thr258Lys
|
|
XM_011539488.1:c.773C>A
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XP_011537790.1:p.Thr258Lys
|
|
NM_001323977.1:c.512C>A
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NP_001310906.1:p.Thr171Lys
|
|
NM_001323978.1:c.512C>A
|
NP_001310907.1:p.Thr171Lys
|
|
NM_001323979.1:c.512C>A
|
NP_001310908.1:p.Thr171Lys
|
|
NM_001323980.1:c.512C>A
|
NP_001310909.1:p.Thr171Lys
|
|
NM_001323981.1:c.773C>A
|
NP_001310910.1:p.Thr258Lys
|
|
XM_017015883.1:c.773C>A
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XP_016871372.1:p.Thr258Lys
|
|
XM_017015884.2:c.773C>A
|
XP_016871373.1:p.Thr258Lys
|
|
XM_024447878.1:c.773C>A
|
XP_024303646.1:p.Thr258Lys
|
|
NM_001323978.2:c.512C>A
|
NP_001310907.1:p.Thr171Lys
|
|
NM_001323979.2:c.512C>A
|
NP_001310908.1:p.Thr171Lys
|
|
NM_001323980.2:c.512C>A
|
NP_001310909.1:p.Thr171Lys
|
|
NM_001323981.2:c.773C>A
|
NP_001310910.1:p.Thr258Lys
|
|
NM_194298.3:c.773C>A
MANE Select
|
NP_919274.1:p.Thr258Lys
|
|