ENST00000377939.5:c.1808G>C
MANE Select
|
ENSP00000367173.4:p.Gly603Ala
|
|
ENST00000377939.4:c.1808G>C
|
ENSP00000367173.4:p.Gly603Ala
|
|
ENST00000483336.1:n.440G>C
|
|
|
ENST00000496676.5:n.1525G>C
|
|
|
NM_207396.2:c.1808G>C
|
NP_997279.2:p.Gly603Ala
|
|
XM_011541439.1:c.1952G>C
|
XP_011539741.1:p.Gly651Ala
|
|
XR_946651.1:n.2301G>C
|
|
|
XR_946652.1:n.2287G>C
|
|
|
XM_011541439.3:c.1952G>C
|
XP_011539741.1:p.Gly651Ala
|
|
XM_017001259.2:c.1874G>C
|
XP_016856748.1:p.Gly625Ala
|
|
XR_001737158.2:n.2386G>C
|
|
|
XR_001737159.2:n.2224G>C
|
|
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XR_001737162.2:n.2320G>C
|
|
|
XR_001737164.2:n.2862G>C
|
|
|
XR_946651.3:n.2158G>C
|
|
|
XR_946652.3:n.2144G>C
|
|
|
NM_207396.3:c.1808G>C
MANE Select
|
NP_997279.2:p.Gly603Ala
|
|