ENST00000371117.8:c.11711A>T
MANE Select
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ENSP00000360158.3:p.Asn3904Ile
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|
ENST00000371117.7:c.11711A>T
|
ENSP00000360158.3:p.Asn3904Ile
|
|
NM_138694.3:c.11711A>T
|
NP_619639.3:p.Asn3904Ile
|
|
XM_011514679.1:c.11711A>T
|
XP_011512981.1:p.Asn3904Ile
|
|
XM_011514680.1:c.11711A>T
|
XP_011512982.1:p.Asn3904Ile
|
|
XM_011514681.1:c.11582A>T
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XP_011512983.1:p.Asn3861Ile
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|
XM_011514682.1:c.11573A>T
|
XP_011512984.1:p.Asn3858Ile
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|
XM_011514683.1:c.11069A>T
|
XP_011512985.1:p.Asn3690Ile
|
|
XM_011514684.1:c.11000A>T
|
XP_011512986.1:p.Asn3667Ile
|
|
XM_011514690.1:c.5786A>T
|
XP_011512992.1:p.Asn1929Ile
|
|
XM_011514691.1:c.5786A>T
|
XP_011512993.1:p.Asn1929Ile
|
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XM_011514680.3:c.11711A>T
|
XP_011512982.1:p.Asn3904Ile
|
|
XM_011514682.3:c.11573A>T
|
XP_011512984.1:p.Asn3858Ile
|
|
XM_011514683.3:c.11069A>T
|
XP_011512985.1:p.Asn3690Ile
|
|
XM_011514684.3:c.11000A>T
|
XP_011512986.1:p.Asn3667Ile
|
|
XM_011514690.3:c.5786A>T
|
XP_011512992.1:p.Asn1929Ile
|
|
XM_011514691.3:c.5786A>T
|
XP_011512993.1:p.Asn1929Ile
|
|
XM_017010944.2:c.11711A>T
|
XP_016866433.1:p.Asn3904Ile
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|
XM_017010945.2:c.11636A>T
|
XP_016866434.1:p.Asn3879Ile
|
|
XM_017010946.2:c.11516A>T
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XP_016866435.1:p.Asn3839Ile
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XM_017010947.2:c.11447A>T
|
XP_016866436.1:p.Asn3816Ile
|
|
XM_017010948.2:c.11000A>T
|
XP_016866437.1:p.Asn3667Ile
|
|
XM_017010949.2:c.9851A>T
|
XP_016866438.1:p.Asn3284Ile
|
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NM_138694.4:c.11711A>T
MANE Select
|
NP_619639.3:p.Asn3904Ile
|
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