ENST00000303941.4:c.1246G>A
MANE Select
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ENSP00000306678.3:p.Ala416Thr
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ENST00000303941.3:c.1246G>A
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ENSP00000306678.3:p.Ala416Thr
|
|
NM_178510.1:c.1246G>A
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NP_848605.1:p.Ala416Thr
|
|
XM_011542736.1:c.1279G>A
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XP_011541038.1:p.Ala427Thr
|
|
XM_011542737.1:c.1249G>A
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XP_011541039.1:p.Ala417Thr
|
|
XM_011542738.1:c.1057G>A
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XP_011541040.1:p.Ala353Thr
|
|
XM_011542736.2:c.1279G>A
|
XP_011541038.1:p.Ala427Thr
|
|
XM_011542737.2:c.1249G>A
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XP_011541039.1:p.Ala417Thr
|
|
XM_011542738.2:c.1057G>A
|
XP_011541040.1:p.Ala353Thr
|
|
XM_017017475.1:c.1276G>A
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XP_016872964.1:p.Ala426Thr
|
|
NM_178510.2:c.1246G>A
MANE Select
|
NP_848605.1:p.Ala416Thr
|
|